|
ENST00000224721.12:c.8239G=
MANE Select
|
ENSP00000224721.9:p.Val2747=
|
|
|
ENST00000642965.1:c.2172G=
|
ENSP00000495222.1:n.2172G=
|
|
|
ENST00000647092.1:c.1836G=
|
ENSP00000495176.1:n.1836G=
|
|
|
ENST00000224721.10:c.8254G=
|
ENSP00000224721.8:p.Val2752=
|
|
|
ENST00000398788.4:c.1519G=
|
ENSP00000381768.3:p.Val507=
|
|
|
ENST00000475158.1:n.1775G=
|
|
|
|
ENST00000619887.4:c.1519G=
|
ENSP00000478374.1:p.Val507=
|
|
|
ENST00000622827.4:c.8239G=
|
ENSP00000483211.1:p.Val2747=
|
|
|
NM_001171933.1:c.1519G=
|
NP_001165404.1:p.Val507=
|
|
|
NM_001171934.1:c.1519G=
|
NP_001165405.1:p.Val507=
|
|
|
NM_022124.5:c.8239G=
|
NP_071407.4:p.Val2747=
|
|
|
XM_006717940.2:c.8434G=
|
XP_006718003.1:p.Val2812=
|
|
|
XM_006717942.2:c.8368G=
|
XP_006718005.1:p.Val2790=
|
|
|
XM_011540039.1:c.8431G=
|
XP_011538341.1:p.Val2811=
|
|
|
XM_011540040.1:c.8428G=
|
XP_011538342.1:p.Val2810=
|
|
|
XM_011540041.1:c.8374G=
|
XP_011538343.1:p.Val2792=
|
|
|
XM_011540042.1:c.8344G=
|
XP_011538344.1:p.Val2782=
|
|
|
XM_011540043.1:c.8434G=
|
XP_011538345.1:p.Val2812=
|
|
|
XM_011540044.1:c.8299G=
|
XP_011538346.1:p.Val2767=
|
|
|
XM_011540045.1:c.8434G=
|
XP_011538347.1:p.Val2812=
|
|
|
XM_011540046.1:c.7894G=
|
XP_011538348.1:p.Val2632=
|
|
|
XM_011540047.1:c.7252G=
|
XP_011538349.1:p.Val2418=
|
|
|
XM_011540052.1:c.4762G=
|
XP_011538354.1:p.Val1588=
|
|
|
NM_022124.6:c.8239G=
MANE Select
|
NP_071407.4:p.Val2747=
|
|
