ENST00000299506.3:c.49G>T
MANE Select
|
ENSP00000299506.3:p.Asp17Tyr
|
|
ENST00000299506.2:c.49G>T
|
ENSP00000299506.2:p.Asp17Tyr
|
|
ENST00000305253.8:c.214G>T
|
ENSP00000305426.4:p.Asp72Tyr
|
|
ENST00000534099.5:c.67G>T
|
ENSP00000434400.1:p.Asp23Tyr
|
|
NM_003320.4:c.214G>T
|
NP_003311.2:p.Asp72Tyr
|
|
NM_177972.2:c.49G>T
|
NP_813977.1:p.Asp17Tyr
|
|
XM_005253109.2:c.175G>T
|
XP_005253166.1:p.Asp59Tyr
|
|
XM_011520344.1:c.85G>T
|
XP_011518646.1:p.Asp29Tyr
|
|
XM_005253109.3:c.175G>T
|
XP_005253166.1:p.Asp59Tyr
|
|
XM_011520344.2:c.85G>T
|
XP_011518646.1:p.Asp29Tyr
|
|
NM_177972.3:c.49G>T
MANE Select
|
NP_813977.1:p.Asp17Tyr
|
|
NM_003320.5:c.214G>T
|
NP_003311.2:p.Asp72Tyr
|
|