ENST00000224721.12:c.7029T>C
MANE Select
|
ENSP00000224721.9:p.Tyr2343=
|
|
ENST00000642965.1:c.962T>C
|
ENSP00000495222.1:n.962T>C
|
|
ENST00000647092.1:c.626T>C
|
ENSP00000495176.1:n.626T>C
|
|
ENST00000224721.10:c.7044T>C
|
ENSP00000224721.8:p.Tyr2348=
|
|
ENST00000398788.4:c.309T>C
|
ENSP00000381768.3:p.Tyr103=
|
|
ENST00000475158.1:n.565T>C
|
|
|
ENST00000619887.4:c.309T>C
|
ENSP00000478374.1:p.Tyr103=
|
|
ENST00000622827.4:c.7029T>C
|
ENSP00000483211.1:p.Tyr2343=
|
|
NM_001171933.1:c.309T>C
|
NP_001165404.1:p.Tyr103=
|
|
NM_001171934.1:c.309T>C
|
NP_001165405.1:p.Tyr103=
|
|
NM_022124.5:c.7029T>C
|
NP_071407.4:p.Tyr2343=
|
|
XM_006717940.2:c.7224T>C
|
XP_006718003.1:p.Tyr2408=
|
|
XM_006717942.2:c.7158T>C
|
XP_006718005.1:p.Tyr2386=
|
|
XM_011540039.1:c.7221T>C
|
XP_011538341.1:p.Tyr2407=
|
|
XM_011540040.1:c.7218T>C
|
XP_011538342.1:p.Tyr2406=
|
|
XM_011540041.1:c.7164T>C
|
XP_011538343.1:p.Tyr2388=
|
|
XM_011540042.1:c.7134T>C
|
XP_011538344.1:p.Tyr2378=
|
|
XM_011540043.1:c.7224T>C
|
XP_011538345.1:p.Tyr2408=
|
|
XM_011540044.1:c.7089T>C
|
XP_011538346.1:p.Tyr2363=
|
|
XM_011540045.1:c.7224T>C
|
XP_011538347.1:p.Tyr2408=
|
|
XM_011540046.1:c.6684T>C
|
XP_011538348.1:p.Tyr2228=
|
|
XM_011540047.1:c.6042T>C
|
XP_011538349.1:p.Tyr2014=
|
|
XM_011540052.1:c.3552T>C
|
XP_011538354.1:p.Tyr1184=
|
|
NM_022124.6:c.7029T>C
MANE Select
|
NP_071407.4:p.Tyr2343=
|
|