ENST00000224721.12:c.7572G>T
MANE Select
|
ENSP00000224721.9:p.Ala2524=
|
|
ENST00000642965.1:c.1505G>T
|
ENSP00000495222.1:n.1505G>T
|
|
ENST00000647092.1:c.1169G>T
|
ENSP00000495176.1:n.1169G>T
|
|
ENST00000224721.10:c.7587G>T
|
ENSP00000224721.8:p.Ala2529=
|
|
ENST00000398788.4:c.852G>T
|
ENSP00000381768.3:p.Ala284=
|
|
ENST00000475158.1:n.1108G>T
|
|
|
ENST00000619887.4:c.852G>T
|
ENSP00000478374.1:p.Ala284=
|
|
ENST00000622827.4:c.7572G>T
|
ENSP00000483211.1:p.Ala2524=
|
|
NM_001171933.1:c.852G>T
|
NP_001165404.1:p.Ala284=
|
|
NM_001171934.1:c.852G>T
|
NP_001165405.1:p.Ala284=
|
|
NM_022124.5:c.7572G>T
|
NP_071407.4:p.Ala2524=
|
|
XM_006717940.2:c.7767G>T
|
XP_006718003.1:p.Ala2589=
|
|
XM_006717942.2:c.7701G>T
|
XP_006718005.1:p.Ala2567=
|
|
XM_011540039.1:c.7764G>T
|
XP_011538341.1:p.Ala2588=
|
|
XM_011540040.1:c.7761G>T
|
XP_011538342.1:p.Ala2587=
|
|
XM_011540041.1:c.7707G>T
|
XP_011538343.1:p.Ala2569=
|
|
XM_011540042.1:c.7677G>T
|
XP_011538344.1:p.Ala2559=
|
|
XM_011540043.1:c.7767G>T
|
XP_011538345.1:p.Ala2589=
|
|
XM_011540044.1:c.7632G>T
|
XP_011538346.1:p.Ala2544=
|
|
XM_011540045.1:c.7767G>T
|
XP_011538347.1:p.Ala2589=
|
|
XM_011540046.1:c.7227G>T
|
XP_011538348.1:p.Ala2409=
|
|
XM_011540047.1:c.6585G>T
|
XP_011538349.1:p.Ala2195=
|
|
XM_011540052.1:c.4095G>T
|
XP_011538354.1:p.Ala1365=
|
|
NM_022124.6:c.7572G>T
MANE Select
|
NP_071407.4:p.Ala2524=
|
|