ENST00000224721.12:c.7294G>T
MANE Select
|
ENSP00000224721.9:p.Gly2432Cys
|
|
ENST00000642965.1:c.1227G>T
|
ENSP00000495222.1:n.1227G>T
|
|
ENST00000647092.1:c.891G>T
|
ENSP00000495176.1:n.891G>T
|
|
ENST00000224721.10:c.7309G>T
|
ENSP00000224721.8:p.Gly2437Cys
|
|
ENST00000398788.4:c.574G>T
|
ENSP00000381768.3:p.Gly192Cys
|
|
ENST00000475158.1:n.830G>T
|
|
|
ENST00000619887.4:c.574G>T
|
ENSP00000478374.1:p.Gly192Cys
|
|
ENST00000622827.4:c.7294G>T
|
ENSP00000483211.1:p.Gly2432Cys
|
|
NM_001171933.1:c.574G>T
|
NP_001165404.1:p.Gly192Cys
|
|
NM_001171934.1:c.574G>T
|
NP_001165405.1:p.Gly192Cys
|
|
NM_022124.5:c.7294G>T
|
NP_071407.4:p.Gly2432Cys
|
|
XM_006717940.2:c.7489G>T
|
XP_006718003.1:p.Gly2497Cys
|
|
XM_006717942.2:c.7423G>T
|
XP_006718005.1:p.Gly2475Cys
|
|
XM_011540039.1:c.7486G>T
|
XP_011538341.1:p.Gly2496Cys
|
|
XM_011540040.1:c.7483G>T
|
XP_011538342.1:p.Gly2495Cys
|
|
XM_011540041.1:c.7429G>T
|
XP_011538343.1:p.Gly2477Cys
|
|
XM_011540042.1:c.7399G>T
|
XP_011538344.1:p.Gly2467Cys
|
|
XM_011540043.1:c.7489G>T
|
XP_011538345.1:p.Gly2497Cys
|
|
XM_011540044.1:c.7354G>T
|
XP_011538346.1:p.Gly2452Cys
|
|
XM_011540045.1:c.7489G>T
|
XP_011538347.1:p.Gly2497Cys
|
|
XM_011540046.1:c.6949G>T
|
XP_011538348.1:p.Gly2317Cys
|
|
XM_011540047.1:c.6307G>T
|
XP_011538349.1:p.Gly2103Cys
|
|
XM_011540052.1:c.3817G>T
|
XP_011538354.1:p.Gly1273Cys
|
|
NM_022124.6:c.7294G>T
MANE Select
|
NP_071407.4:p.Gly2432Cys
|
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