ENST00000224721.12:c.6976G>A
MANE Select
|
ENSP00000224721.9:p.Gly2326Ser
|
|
ENST00000642965.1:c.909G>A
|
ENSP00000495222.1:n.909G>A
|
|
ENST00000647092.1:c.573G>A
|
ENSP00000495176.1:n.573G>A
|
|
ENST00000224721.10:c.6991G>A
|
ENSP00000224721.8:p.Gly2331Ser
|
|
ENST00000398788.4:c.256G>A
|
ENSP00000381768.3:p.Gly86Ser
|
|
ENST00000475158.1:n.512G>A
|
|
|
ENST00000619887.4:c.256G>A
|
ENSP00000478374.1:p.Gly86Ser
|
|
ENST00000622827.4:c.6976G>A
|
ENSP00000483211.1:p.Gly2326Ser
|
|
NM_001171933.1:c.256G>A
|
NP_001165404.1:p.Gly86Ser
|
|
NM_001171934.1:c.256G>A
|
NP_001165405.1:p.Gly86Ser
|
|
NM_022124.5:c.6976G>A
|
NP_071407.4:p.Gly2326Ser
|
|
XM_006717940.2:c.7171G>A
|
XP_006718003.1:p.Gly2391Ser
|
|
XM_006717942.2:c.7105G>A
|
XP_006718005.1:p.Gly2369Ser
|
|
XM_011540039.1:c.7168G>A
|
XP_011538341.1:p.Gly2390Ser
|
|
XM_011540040.1:c.7165G>A
|
XP_011538342.1:p.Gly2389Ser
|
|
XM_011540041.1:c.7111G>A
|
XP_011538343.1:p.Gly2371Ser
|
|
XM_011540042.1:c.7081G>A
|
XP_011538344.1:p.Gly2361Ser
|
|
XM_011540043.1:c.7171G>A
|
XP_011538345.1:p.Gly2391Ser
|
|
XM_011540044.1:c.7036G>A
|
XP_011538346.1:p.Gly2346Ser
|
|
XM_011540045.1:c.7171G>A
|
XP_011538347.1:p.Gly2391Ser
|
|
XM_011540046.1:c.6631G>A
|
XP_011538348.1:p.Gly2211Ser
|
|
XM_011540047.1:c.5989G>A
|
XP_011538349.1:p.Gly1997Ser
|
|
XM_011540052.1:c.3499G>A
|
XP_011538354.1:p.Gly1167Ser
|
|
NM_022124.6:c.6976G>A
MANE Select
|
NP_071407.4:p.Gly2326Ser
|
|