ENST00000299084.9:c.1129T>C
MANE Select
|
ENSP00000299084.4:p.Tyr377His
|
|
ENST00000299084.8:c.1129T>C
|
ENSP00000299084.4:p.Tyr377His
|
|
NM_152594.2:c.1129T>C
|
NP_689807.1:p.Tyr377His
|
|
XM_005254202.2:c.1165T>C
|
XP_005254259.1:p.Tyr389His
|
|
XM_005254203.3:c.907T>C
|
XP_005254260.1:p.Tyr303His
|
|
XM_011521288.1:c.1066T>C
|
XP_011519590.1:p.Tyr356His
|
|
XM_011521289.1:c.1066T>C
|
XP_011519591.1:p.Tyr356His
|
|
XM_011521290.1:c.1066T>C
|
XP_011519592.1:p.Tyr356His
|
|
XM_005254202.3:c.1165T>C
|
XP_005254259.1:p.Tyr389His
|
|
XM_011521289.3:c.1066T>C
|
XP_011519591.1:p.Tyr356His
|
|
NM_152594.3:c.1129T>C
MANE Select
|
NP_689807.1:p.Tyr377His
|
|