NM_001042428.2:c.1429C>T
MANE Select
|
NP_001035893.1:p.His477Tyr
|
ENST00000219091.9:c.1429C>T
MANE Select
|
ENSP00000219091.4:p.His477Tyr
|
NM_001042428.1:c.1429C>T
|
NP_001035893.1:p.His477Tyr
|
NM_001278158.1:c.1429C>T
|
NP_001265087.1:p.His477Tyr
|
NM_001278158.2:c.1429C>T
|
NP_001265087.1:p.His477Tyr
|
NM_003456.2:c.1429C>T
|
NP_003447.2:p.His477Tyr
|
NM_003456.3:c.1429C>T
|
NP_003447.2:p.His477Tyr
|
ENST00000219091.8:c.1429C>T
|
ENSP00000219091.4:p.His477Tyr
|
ENST00000382192.7:c.1429C>T
|
ENSP00000371627.3:p.His477Tyr
|
ENST00000620094.4:c.1429C>T
|
ENSP00000480401.1:p.His477Tyr
|
XM_005255558.1:c.1429C>T
|
XP_005255615.1:p.His477Tyr
|
XM_005255558.2:c.1429C>T
|
XP_005255615.1:p.His477Tyr
|