ENST00000224721.12:c.8779T>C
MANE Select
|
ENSP00000224721.9:p.Tyr2927His
|
|
ENST00000642965.1:c.2712T>C
|
ENSP00000495222.1:n.2712T>C
|
|
ENST00000647092.1:c.2376T>C
|
ENSP00000495176.1:n.2376T>C
|
|
ENST00000224721.10:c.8794T>C
|
ENSP00000224721.8:p.Tyr2932His
|
|
ENST00000398788.4:c.2059T>C
|
ENSP00000381768.3:p.Tyr687His
|
|
ENST00000475158.1:n.2315T>C
|
|
|
ENST00000619887.4:c.2059T>C
|
ENSP00000478374.1:p.Tyr687His
|
|
ENST00000622827.4:c.8779T>C
|
ENSP00000483211.1:p.Tyr2927His
|
|
NM_001171933.1:c.2059T>C
|
NP_001165404.1:p.Tyr687His
|
|
NM_001171934.1:c.2059T>C
|
NP_001165405.1:p.Tyr687His
|
|
NM_022124.5:c.8779T>C
|
NP_071407.4:p.Tyr2927His
|
|
XM_006717940.2:c.8974T>C
|
XP_006718003.1:p.Tyr2992His
|
|
XM_006717942.2:c.8908T>C
|
XP_006718005.1:p.Tyr2970His
|
|
XM_011540039.1:c.8971T>C
|
XP_011538341.1:p.Tyr2991His
|
|
XM_011540040.1:c.8968T>C
|
XP_011538342.1:p.Tyr2990His
|
|
XM_011540041.1:c.8914T>C
|
XP_011538343.1:p.Tyr2972His
|
|
XM_011540042.1:c.8884T>C
|
XP_011538344.1:p.Tyr2962His
|
|
XM_011540043.1:c.8974T>C
|
XP_011538345.1:p.Tyr2992His
|
|
XM_011540044.1:c.8839T>C
|
XP_011538346.1:p.Tyr2947His
|
|
XM_011540045.1:c.8974T>C
|
XP_011538347.1:p.Tyr2992His
|
|
XM_011540046.1:c.8434T>C
|
XP_011538348.1:p.Tyr2812His
|
|
XM_011540047.1:c.7792T>C
|
XP_011538349.1:p.Tyr2598His
|
|
XM_011540052.1:c.5302T>C
|
XP_011538354.1:p.Tyr1768His
|
|
NM_022124.6:c.8779T>C
MANE Select
|
NP_071407.4:p.Tyr2927His
|
|