ENST00000224721.12:c.7366G>C
MANE Select
|
ENSP00000224721.9:p.Asp2456His
|
|
ENST00000642965.1:c.1299G>C
|
ENSP00000495222.1:n.1299G>C
|
|
ENST00000647092.1:c.963G>C
|
ENSP00000495176.1:n.963G>C
|
|
ENST00000224721.10:c.7381G>C
|
ENSP00000224721.8:p.Asp2461His
|
|
ENST00000398788.4:c.646G>C
|
ENSP00000381768.3:p.Asp216His
|
|
ENST00000475158.1:n.902G>C
|
|
|
ENST00000619887.4:c.646G>C
|
ENSP00000478374.1:p.Asp216His
|
|
ENST00000622827.4:c.7366G>C
|
ENSP00000483211.1:p.Asp2456His
|
|
NM_001171933.1:c.646G>C
|
NP_001165404.1:p.Asp216His
|
|
NM_001171934.1:c.646G>C
|
NP_001165405.1:p.Asp216His
|
|
NM_022124.5:c.7366G>C
|
NP_071407.4:p.Asp2456His
|
|
XM_006717940.2:c.7561G>C
|
XP_006718003.1:p.Asp2521His
|
|
XM_006717942.2:c.7495G>C
|
XP_006718005.1:p.Asp2499His
|
|
XM_011540039.1:c.7558G>C
|
XP_011538341.1:p.Asp2520His
|
|
XM_011540040.1:c.7555G>C
|
XP_011538342.1:p.Asp2519His
|
|
XM_011540041.1:c.7501G>C
|
XP_011538343.1:p.Asp2501His
|
|
XM_011540042.1:c.7471G>C
|
XP_011538344.1:p.Asp2491His
|
|
XM_011540043.1:c.7561G>C
|
XP_011538345.1:p.Asp2521His
|
|
XM_011540044.1:c.7426G>C
|
XP_011538346.1:p.Asp2476His
|
|
XM_011540045.1:c.7561G>C
|
XP_011538347.1:p.Asp2521His
|
|
XM_011540046.1:c.7021G>C
|
XP_011538348.1:p.Asp2341His
|
|
XM_011540047.1:c.6379G>C
|
XP_011538349.1:p.Asp2127His
|
|
XM_011540052.1:c.3889G>C
|
XP_011538354.1:p.Asp1297His
|
|
NM_022124.6:c.7366G>C
MANE Select
|
NP_071407.4:p.Asp2456His
|
|