ENST00000372470.9:c.289G>T
MANE Select
|
ENSP00000361548.3:p.Asp97Tyr
|
|
ENST00000413998.7:c.268G>T
|
ENSP00000414004.3:p.Asp90Tyr
|
|
ENST00000638732.1:n.289G>T
|
|
|
ENST00000372470.7:c.289G>T
|
ENSP00000361548.3:p.Asp97Tyr
|
|
ENST00000413998.6:c.289G>T
|
ENSP00000414004.2:p.Asp97Tyr
|
|
ENST00000612993.1:c.289G>T
|
ENSP00000480273.1:p.Asp97Tyr
|
|
NM_005373.2:c.289G>T , LRG_510t1:c.289G>T
|
NP_005364.1:p.Asp97Tyr
|
|
XM_011541478.1:c.268G>T
|
XP_011539780.1:p.Asp90Tyr
|
|
XM_017001320.1:c.460G>T
|
XP_016856809.1:p.Asp154Tyr
|
|
NM_005373.3:c.289G>T
MANE Select
|
NP_005364.1:p.Asp97Tyr
|
|