ENST00000255531.8:c.2575G>T
|
ENSP00000255531.7:p.Asp859Tyr
|
|
ENST00000373034.8:c.2716G>T
MANE Select
|
ENSP00000362125.4:p.Asp906Tyr
|
|
ENST00000420881.6:c.2572G>T
|
ENSP00000400327.2:p.Asp858Tyr
|
|
NM_001105243.1:c.2575G>T
|
NP_001098713.1:p.Asp859Tyr
|
|
NM_001184880.1:c.2716G>T
|
NP_001171809.1:p.Asp906Tyr
|
|
NM_020766.2:c.2572G>T
|
NP_065817.2:p.Asp858Tyr
|
|
XM_011530997.1:c.2713G>T
|
XP_011529299.1:p.Asp905Tyr
|
|
XM_011530997.2:c.2713G>T
|
XP_011529299.1:p.Asp905Tyr
|
|
NM_001105243.2:c.2575G>T
|
NP_001098713.1:p.Asp859Tyr
|
|
NM_001184880.2:c.2716G>T
MANE Select
|
NP_001171809.1:p.Asp906Tyr
|
|
NM_020766.3:c.2572G>T
|
NP_065817.2:p.Asp858Tyr
|
|