|
ENST00000346322.10:c.4755-2652C>T
(MYLK)
|
ENSP00000320622.6:n.4755-2652C>T
|
|
|
ENST00000508240.2:c.1395C>T
(MYLK)
|
ENSP00000422984.2:p.Asn465=
|
|
|
ENST00000684879.1:n.2627C>T
(MYLK)
|
|
|
|
ENST00000685021.1:c.2229C>T
(MYLK)
|
ENSP00000508447.1:p.Asn743=
|
|
|
ENST00000685170.1:n.208C>T
(MYLK)
|
|
|
|
ENST00000685259.1:c.2514C>T
(MYLK)
|
|
|
|
ENST00000685907.1:n.2776C>T
(MYLK)
|
|
|
|
ENST00000685953.1:c.1395C>T
(MYLK)
|
ENSP00000510593.1:p.Asn465=
|
|
|
ENST00000686039.1:c.2379C>T
(MYLK)
|
|
|
|
ENST00000686245.1:c.2112C>T
(MYLK)
|
ENSP00000509313.1:p.Asn704=
|
|
|
ENST00000686281.1:n.287C>T
(MYLK)
|
|
|
|
ENST00000686406.1:c.4995C>T
(MYLK)
|
ENSP00000509044.1:p.Asn1665=
|
|
|
ENST00000686458.1:n.1497C>T
(MYLK)
|
|
|
|
ENST00000686761.1:c.4995C>T
(MYLK)
|
ENSP00000508758.1:p.Asn1665=
|
|
|
ENST00000686822.1:n.4889C>T
(MYLK)
|
|
|
|
ENST00000687434.1:c.*1211C>T
(MYLK)
|
ENSP00000509751.1:n.*1211C>T
|
|
|
ENST00000687709.1:n.3050C>T
(MYLK)
|
|
|
|
ENST00000687848.1:c.5025C>T
(MYLK)
|
ENSP00000508761.1:p.Asn1675=
|
|
|
ENST00000688024.1:c.2229C>T
(MYLK)
|
ENSP00000509803.1:p.Asn743=
|
|
|
ENST00000688223.1:c.2025C>T
(MYLK)
|
ENSP00000508935.1:p.Asn675=
|
|
|
ENST00000689446.1:n.200C>T
(MYLK)
|
|
|
|
ENST00000689868.1:n.2723C>T
(MYLK)
|
|
|
|
ENST00000689918.1:n.1070C>T
(MYLK)
|
|
|
|
ENST00000690086.1:n.1096C>T
(MYLK)
|
|
|
|
ENST00000690167.1:n.2666C>T
(MYLK)
|
|
|
|
ENST00000690457.1:c.4233C>T
(MYLK)
|
ENSP00000508777.1:p.Asn1411=
|
|
|
ENST00000690534.1:n.1516C>T
(MYLK)
|
|
|
|
ENST00000691933.1:c.2619C>T
(MYLK)
|
|
|
|
ENST00000692811.1:n.445C>T
(MYLK)
|
|
|
|
ENST00000693689.1:c.4788C>T
(MYLK)
|
ENSP00000510503.1:p.Asn1596=
|
|
|
ENST00000360304.8:c.4995C>T
(MYLK)
MANE Select
|
ENSP00000353452.3:p.Asn1665=
|
|
|
ENST00000346322.9:c.4788C>T
(MYLK)
|
ENSP00000320622.5:p.Asn1596=
|
|
|
ENST00000354792.9:c.4788C>T
(MYLK)
|
ENSP00000346846.6:p.Asn1596=
|
|
|
ENST00000359169.5:c.4962-2652C>T
(MYLK)
|
ENSP00000352088.1:n.4962-2652C>T
|
|
|
ENST00000360304.7:c.4995C>T
(MYLK)
|
ENSP00000353452.3:p.Asn1665=
|
|
|
ENST00000360772.7:c.4962-2652C>T
(MYLK)
|
ENSP00000354004.3:n.4962-2652C>T
|
|
|
ENST00000464489.5:c.*4574C>T
(MYLK)
|
ENSP00000417798.1:n.*4574C>T
|
|
|
ENST00000475616.5:c.4995C>T
(MYLK)
|
ENSP00000418335.1:p.Asn1665=
|
|
|
NM_053025.3:c.4995C>T
(MYLK)
|
NP_444253.3:p.Asn1665=
|
|
|
NM_053026.3:c.4788C>T
(MYLK)
|
NP_444254.3:p.Asn1596=
|
|
|
NM_053027.3:c.4962-2652C>T
(MYLK)
|
NP_444255.3:n.4962-2652C>T
|
|
|
NM_053028.3:c.4755-2652C>T
(MYLK)
|
NP_444256.3:n.4755-2652C>T
|
|
|
NR_038266.2:n.389G>A
(MYLK-AS1)
|
|
|
|
NR_121654.1:n.296G>A
(MYLK-AS1)
|
|
|
|
XM_011512860.1:c.4995C>T
(MYLK)
|
XP_011511162.1:p.Asn1665=
|
|
|
XM_011512861.1:c.4791C>T
(MYLK)
|
XP_011511163.1:p.Asn1597=
|
|
|
XM_011512862.1:c.4467C>T
(MYLK)
|
XP_011511164.1:p.Asn1489=
|
|
|
NM_001321309.1:c.4467C>T
(MYLK)
|
NP_001308238.1:p.Asn1489=
|
|
|
XM_011512860.3:c.5025C>T
(MYLK)
|
XP_011511162.2:p.Asn1675=
|
|
|
XM_011512861.3:c.4821C>T
(MYLK)
|
XP_011511163.2:p.Asn1607=
|
|
|
XM_017006469.2:c.2229C>T
(MYLK)
|
XP_016861958.1:p.Asn743=
|
|
|
XM_017006470.2:c.1395C>T
(MYLK)
|
XP_016861959.1:p.Asn465=
|
|
|
XM_017006471.2:c.1395C>T
(MYLK)
|
XP_016861960.1:p.Asn465=
|
|
|
XM_024453532.1:c.5025C>T
(MYLK)
|
XP_024309300.1:p.Asn1675=
|
|
|
XM_024453533.1:c.4995C>T
(MYLK)
|
XP_024309301.1:p.Asn1665=
|
|
|
XM_024453534.1:c.4818C>T
(MYLK)
|
XP_024309302.1:p.Asn1606=
|
|
|
XM_024453535.1:c.4788C>T
(MYLK)
|
XP_024309303.1:p.Asn1596=
|
|
|
XM_024453536.1:c.4995C>T
(MYLK)
|
XP_024309304.1:p.Asn1665=
|
|
|
XM_024453537.1:c.4995C>T
(MYLK)
|
XP_024309305.1:p.Asn1665=
|
|
|
NM_001321309.2:c.4467C>T
(MYLK)
|
NP_001308238.1:p.Asn1489=
|
|
|
NM_053025.4:c.4995C>T
(MYLK)
MANE Select
|
NP_444253.3:p.Asn1665=
|
|
|
NM_053026.4:c.4788C>T
(MYLK)
|
NP_444254.3:p.Asn1596=
|
|
|
NM_053027.4:c.4962-2652C>T
(MYLK)
|
NP_444255.3:n.4962-2652C>T
|
|
|
NM_053028.4:c.4755-2652C>T
(MYLK)
|
NP_444256.3:n.4755-2652C>T
|
|
