|
ENST00000346322.10:c.4761C>T
(MYLK)
|
ENSP00000320622.6:p.Arg1587=
|
|
|
ENST00000508240.2:c.1521C>T
(MYLK)
|
ENSP00000422984.2:p.Arg507=
|
|
|
ENST00000684879.1:n.2753C>T
(MYLK)
|
|
|
|
ENST00000685021.1:c.2355C>T
(MYLK)
|
ENSP00000508447.1:p.Arg785=
|
|
|
ENST00000685170.1:n.334C>T
(MYLK)
|
|
|
|
ENST00000685259.1:c.2640C>T
(MYLK)
|
|
|
|
ENST00000685907.1:n.2902C>T
(MYLK)
|
|
|
|
ENST00000685953.1:c.1521C>T
(MYLK)
|
ENSP00000510593.1:p.Arg507=
|
|
|
ENST00000686039.1:c.2505C>T
(MYLK)
|
|
|
|
ENST00000686245.1:c.2238C>T
(MYLK)
|
ENSP00000509313.1:p.Arg746=
|
|
|
ENST00000686281.1:n.413C>T
(MYLK)
|
|
|
|
ENST00000686406.1:c.5121C>T
(MYLK)
|
ENSP00000509044.1:p.Arg1707=
|
|
|
ENST00000686458.1:n.1623C>T
(MYLK)
|
|
|
|
ENST00000686761.1:c.5121C>T
(MYLK)
|
ENSP00000508758.1:p.Arg1707=
|
|
|
ENST00000686822.1:n.5015C>T
(MYLK)
|
|
|
|
ENST00000687434.1:c.*1337C>T
(MYLK)
|
ENSP00000509751.1:n.*1337C>T
|
|
|
ENST00000687709.1:n.3176C>T
(MYLK)
|
|
|
|
ENST00000687848.1:c.5151C>T
(MYLK)
|
ENSP00000508761.1:p.Arg1717=
|
|
|
ENST00000688024.1:c.2355C>T
(MYLK)
|
ENSP00000509803.1:p.Arg785=
|
|
|
ENST00000688223.1:c.2151C>T
(MYLK)
|
ENSP00000508935.1:p.Arg717=
|
|
|
ENST00000689446.1:n.326C>T
(MYLK)
|
|
|
|
ENST00000689868.1:n.5381C>T
(MYLK)
|
|
|
|
ENST00000689918.1:n.1196C>T
(MYLK)
|
|
|
|
ENST00000690086.1:n.1222C>T
(MYLK)
|
|
|
|
ENST00000690167.1:n.2792C>T
(MYLK)
|
|
|
|
ENST00000690457.1:c.4359C>T
(MYLK)
|
ENSP00000508777.1:p.Arg1453=
|
|
|
ENST00000690534.1:n.1642C>T
(MYLK)
|
|
|
|
ENST00000691933.1:c.2745C>T
(MYLK)
|
|
|
|
ENST00000692811.1:n.571C>T
(MYLK)
|
|
|
|
ENST00000693689.1:c.4914C>T
(MYLK)
|
ENSP00000510503.1:p.Arg1638=
|
|
|
ENST00000360304.8:c.5121C>T
(MYLK)
MANE Select
|
ENSP00000353452.3:p.Arg1707=
|
|
|
ENST00000346322.9:c.4914C>T
(MYLK)
|
ENSP00000320622.5:p.Arg1638=
|
|
|
ENST00000354792.9:c.4914C>T
(MYLK)
|
ENSP00000346846.6:p.Arg1638=
|
|
|
ENST00000359169.5:c.4968C>T
(MYLK)
|
ENSP00000352088.1:p.Arg1656=
|
|
|
ENST00000360304.7:c.5121C>T
(MYLK)
|
ENSP00000353452.3:p.Arg1707=
|
|
|
ENST00000360772.7:c.4968C>T
(MYLK)
|
ENSP00000354004.3:p.Arg1656=
|
|
|
ENST00000464489.5:c.*4700C>T
(MYLK)
|
ENSP00000417798.1:n.*4700C>T
|
|
|
ENST00000475616.5:c.5121C>T
(MYLK)
|
ENSP00000418335.1:p.Arg1707=
|
|
|
NM_053025.3:c.5121C>T
(MYLK)
|
NP_444253.3:p.Arg1707=
|
|
|
NM_053026.3:c.4914C>T
(MYLK)
|
NP_444254.3:p.Arg1638=
|
|
|
NM_053027.3:c.4968C>T
(MYLK)
|
NP_444255.3:p.Arg1656=
|
|
|
NM_053028.3:c.4761C>T
(MYLK)
|
NP_444256.3:p.Arg1587=
|
|
|
NR_038266.2:n.290-2559G>A
(MYLK-AS1)
|
|
|
|
NR_121654.1:n.197-2559G>A
(MYLK-AS1)
|
|
|
|
XM_011512860.1:c.5121C>T
(MYLK)
|
XP_011511162.1:p.Arg1707=
|
|
|
XM_011512861.1:c.4917C>T
(MYLK)
|
XP_011511163.1:p.Arg1639=
|
|
|
XM_011512862.1:c.4593C>T
(MYLK)
|
XP_011511164.1:p.Arg1531=
|
|
|
NM_001321309.1:c.4593C>T
(MYLK)
|
NP_001308238.1:p.Arg1531=
|
|
|
XM_011512860.3:c.5151C>T
(MYLK)
|
XP_011511162.2:p.Arg1717=
|
|
|
XM_011512861.3:c.4947C>T
(MYLK)
|
XP_011511163.2:p.Arg1649=
|
|
|
XM_017006469.2:c.2355C>T
(MYLK)
|
XP_016861958.1:p.Arg785=
|
|
|
XM_017006470.2:c.1521C>T
(MYLK)
|
XP_016861959.1:p.Arg507=
|
|
|
XM_017006471.2:c.1521C>T
(MYLK)
|
XP_016861960.1:p.Arg507=
|
|
|
XM_024453532.1:c.5151C>T
(MYLK)
|
XP_024309300.1:p.Arg1717=
|
|
|
XM_024453533.1:c.5121C>T
(MYLK)
|
XP_024309301.1:p.Arg1707=
|
|
|
XM_024453534.1:c.4944C>T
(MYLK)
|
XP_024309302.1:p.Arg1648=
|
|
|
XM_024453535.1:c.4914C>T
(MYLK)
|
XP_024309303.1:p.Arg1638=
|
|
|
XM_024453536.1:c.5121C>T
(MYLK)
|
XP_024309304.1:p.Arg1707=
|
|
|
XM_024453537.1:c.5121C>T
(MYLK)
|
XP_024309305.1:p.Arg1707=
|
|
|
NM_001321309.2:c.4593C>T
(MYLK)
|
NP_001308238.1:p.Arg1531=
|
|
|
NM_053025.4:c.5121C>T
(MYLK)
MANE Select
|
NP_444253.3:p.Arg1707=
|
|
|
NM_053026.4:c.4914C>T
(MYLK)
|
NP_444254.3:p.Arg1638=
|
|
|
NM_053027.4:c.4968C>T
(MYLK)
|
NP_444255.3:p.Arg1656=
|
|
|
NM_053028.4:c.4761C>T
(MYLK)
|
NP_444256.3:p.Arg1587=
|
|
