ENST00000346322.10:c.4262G=
|
ENSP00000320622.6:p.Trp1421=
|
|
ENST00000508240.2:c.869G=
|
ENSP00000422984.2:p.Trp290=
|
|
ENST00000513111.2:n.599G=
|
|
|
ENST00000684879.1:n.2101G=
|
|
|
ENST00000685021.1:c.1703G=
|
ENSP00000508447.1:p.Trp568=
|
|
ENST00000685259.1:c.1988G=
|
|
|
ENST00000685907.1:n.2250G=
|
|
|
ENST00000685953.1:c.869G=
|
ENSP00000510593.1:p.Trp290=
|
|
ENST00000686039.1:c.1853G=
|
|
|
ENST00000686245.1:c.1586G=
|
ENSP00000509313.1:p.Trp529=
|
|
ENST00000686406.1:c.4469G=
|
ENSP00000509044.1:p.Trp1490=
|
|
ENST00000686458.1:n.971G=
|
|
|
ENST00000686761.1:c.4469G=
|
ENSP00000508758.1:p.Trp1490=
|
|
ENST00000686822.1:n.4363G=
|
|
|
ENST00000687434.1:c.*685G=
|
ENSP00000509751.1:n.*685G=
|
|
ENST00000687709.1:n.2524G=
|
|
|
ENST00000687848.1:c.4499G=
|
ENSP00000508761.1:p.Trp1500=
|
|
ENST00000688024.1:c.1703G=
|
ENSP00000509803.1:p.Trp568=
|
|
ENST00000688223.1:c.1649+1597G=
|
ENSP00000508935.1:n.1649+1597G=
|
|
ENST00000689868.1:n.2197G=
|
|
|
ENST00000689918.1:n.544G=
|
|
|
ENST00000690086.1:n.570G=
|
|
|
ENST00000690167.1:n.2140G=
|
|
|
ENST00000690457.1:c.3707G=
|
ENSP00000508777.1:p.Trp1236=
|
|
ENST00000690534.1:n.990G=
|
|
|
ENST00000691933.1:c.2093G=
|
|
|
ENST00000692352.1:c.2007G=
|
|
|
ENST00000693689.1:c.4262G=
|
ENSP00000510503.1:p.Trp1421=
|
|
ENST00000360304.8:c.4469G=
MANE Select
|
ENSP00000353452.3:p.Trp1490=
|
|
ENST00000346322.9:c.4262G=
|
ENSP00000320622.5:p.Trp1421=
|
|
ENST00000354792.9:c.4262G=
|
ENSP00000346846.6:p.Trp1421=
|
|
ENST00000359169.5:c.4469G=
|
ENSP00000352088.1:p.Trp1490=
|
|
ENST00000360304.7:c.4469G=
|
ENSP00000353452.3:p.Trp1490=
|
|
ENST00000360772.7:c.4469G=
|
ENSP00000354004.3:p.Trp1490=
|
|
ENST00000464489.5:c.*4048G=
|
ENSP00000417798.1:n.*4048G=
|
|
ENST00000475616.5:c.4469G=
|
ENSP00000418335.1:p.Trp1490=
|
|
ENST00000513111.1:n.181G=
|
|
|
ENST00000514895.5:n.94+1597G=
|
|
|
NM_053025.3:c.4469G=
|
NP_444253.3:p.Trp1490=
|
|
NM_053026.3:c.4262G=
|
NP_444254.3:p.Trp1421=
|
|
NM_053027.3:c.4469G=
|
NP_444255.3:p.Trp1490=
|
|
NM_053028.3:c.4262G=
|
NP_444256.3:p.Trp1421=
|
|
XM_011512860.1:c.4469G=
|
XP_011511162.1:p.Trp1490=
|
|
XM_011512861.1:c.4415+1597G=
|
XP_011511163.1:n.4415+1597G=
|
|
XM_011512862.1:c.3941G=
|
XP_011511164.1:p.Trp1314=
|
|
NM_001321309.1:c.3941G=
|
NP_001308238.1:p.Trp1314=
|
|
XM_011512860.3:c.4499G=
|
XP_011511162.2:p.Trp1500=
|
|
XM_011512861.3:c.4445+1597G=
|
XP_011511163.2:n.4445+1597G=
|
|
XM_017006469.2:c.1703G=
|
XP_016861958.1:p.Trp568=
|
|
XM_017006470.2:c.869G=
|
XP_016861959.1:p.Trp290=
|
|
XM_017006471.2:c.869G=
|
XP_016861960.1:p.Trp290=
|
|
XM_024453532.1:c.4499G=
|
XP_024309300.1:p.Trp1500=
|
|
XM_024453533.1:c.4469G=
|
XP_024309301.1:p.Trp1490=
|
|
XM_024453534.1:c.4292G=
|
XP_024309302.1:p.Trp1431=
|
|
XM_024453535.1:c.4262G=
|
XP_024309303.1:p.Trp1421=
|
|
XM_024453536.1:c.4469G=
|
XP_024309304.1:p.Trp1490=
|
|
XM_024453537.1:c.4469G=
|
XP_024309305.1:p.Trp1490=
|
|
NM_001321309.2:c.3941G=
|
NP_001308238.1:p.Trp1314=
|
|
NM_053025.4:c.4469G=
MANE Select
|
NP_444253.3:p.Trp1490=
|
|
NM_053026.4:c.4262G=
|
NP_444254.3:p.Trp1421=
|
|
NM_053027.4:c.4469G=
|
NP_444255.3:p.Trp1490=
|
|
NM_053028.4:c.4262G=
|
NP_444256.3:p.Trp1421=
|
|