ENST00000224721.12:c.8312G>T
MANE Select
|
ENSP00000224721.9:p.Gly2771Val
|
|
ENST00000642965.1:c.2245G>T
|
ENSP00000495222.1:n.2245G>T
|
|
ENST00000647092.1:c.1909G>T
|
ENSP00000495176.1:n.1909G>T
|
|
ENST00000224721.10:c.8327G>T
|
ENSP00000224721.8:p.Gly2776Val
|
|
ENST00000398788.4:c.1592G>T
|
ENSP00000381768.3:p.Gly531Val
|
|
ENST00000475158.1:n.1848G>T
|
|
|
ENST00000619887.4:c.1592G>T
|
ENSP00000478374.1:p.Gly531Val
|
|
ENST00000622827.4:c.8312G>T
|
ENSP00000483211.1:p.Gly2771Val
|
|
NM_001171933.1:c.1592G>T
|
NP_001165404.1:p.Gly531Val
|
|
NM_001171934.1:c.1592G>T
|
NP_001165405.1:p.Gly531Val
|
|
NM_022124.5:c.8312G>T
|
NP_071407.4:p.Gly2771Val
|
|
XM_006717940.2:c.8507G>T
|
XP_006718003.1:p.Gly2836Val
|
|
XM_006717942.2:c.8441G>T
|
XP_006718005.1:p.Gly2814Val
|
|
XM_011540039.1:c.8504G>T
|
XP_011538341.1:p.Gly2835Val
|
|
XM_011540040.1:c.8501G>T
|
XP_011538342.1:p.Gly2834Val
|
|
XM_011540041.1:c.8447G>T
|
XP_011538343.1:p.Gly2816Val
|
|
XM_011540042.1:c.8417G>T
|
XP_011538344.1:p.Gly2806Val
|
|
XM_011540043.1:c.8507G>T
|
XP_011538345.1:p.Gly2836Val
|
|
XM_011540044.1:c.8372G>T
|
XP_011538346.1:p.Gly2791Val
|
|
XM_011540045.1:c.8507G>T
|
XP_011538347.1:p.Gly2836Val
|
|
XM_011540046.1:c.7967G>T
|
XP_011538348.1:p.Gly2656Val
|
|
XM_011540047.1:c.7325G>T
|
XP_011538349.1:p.Gly2442Val
|
|
XM_011540052.1:c.4835G>T
|
XP_011538354.1:p.Gly1612Val
|
|
NM_022124.6:c.8312G>T
MANE Select
|
NP_071407.4:p.Gly2771Val
|
|