ENST00000224721.12:c.8413G>T
MANE Select
|
ENSP00000224721.9:p.Ala2805Ser
|
|
ENST00000642965.1:c.2346G>T
|
ENSP00000495222.1:n.2346G>T
|
|
ENST00000647092.1:c.2010G>T
|
ENSP00000495176.1:n.2010G>T
|
|
ENST00000224721.10:c.8428G>T
|
ENSP00000224721.8:p.Ala2810Ser
|
|
ENST00000398788.4:c.1693G>T
|
ENSP00000381768.3:p.Ala565Ser
|
|
ENST00000475158.1:n.1949G>T
|
|
|
ENST00000619887.4:c.1693G>T
|
ENSP00000478374.1:p.Ala565Ser
|
|
ENST00000622827.4:c.8413G>T
|
ENSP00000483211.1:p.Ala2805Ser
|
|
NM_001171933.1:c.1693G>T
|
NP_001165404.1:p.Ala565Ser
|
|
NM_001171934.1:c.1693G>T
|
NP_001165405.1:p.Ala565Ser
|
|
NM_022124.5:c.8413G>T
|
NP_071407.4:p.Ala2805Ser
|
|
XM_006717940.2:c.8608G>T
|
XP_006718003.1:p.Ala2870Ser
|
|
XM_006717942.2:c.8542G>T
|
XP_006718005.1:p.Ala2848Ser
|
|
XM_011540039.1:c.8605G>T
|
XP_011538341.1:p.Ala2869Ser
|
|
XM_011540040.1:c.8602G>T
|
XP_011538342.1:p.Ala2868Ser
|
|
XM_011540041.1:c.8548G>T
|
XP_011538343.1:p.Ala2850Ser
|
|
XM_011540042.1:c.8518G>T
|
XP_011538344.1:p.Ala2840Ser
|
|
XM_011540043.1:c.8608G>T
|
XP_011538345.1:p.Ala2870Ser
|
|
XM_011540044.1:c.8473G>T
|
XP_011538346.1:p.Ala2825Ser
|
|
XM_011540045.1:c.8608G>T
|
XP_011538347.1:p.Ala2870Ser
|
|
XM_011540046.1:c.8068G>T
|
XP_011538348.1:p.Ala2690Ser
|
|
XM_011540047.1:c.7426G>T
|
XP_011538349.1:p.Ala2476Ser
|
|
XM_011540052.1:c.4936G>T
|
XP_011538354.1:p.Ala1646Ser
|
|
NM_022124.6:c.8413G>T
MANE Select
|
NP_071407.4:p.Ala2805Ser
|
|