ENST00000264613.11:c.2054T>A
MANE Select
|
ENSP00000264613.6:p.Leu685His
|
|
ENST00000264613.10:c.2054T>A
|
ENSP00000264613.6:p.Leu685His
|
|
ENST00000462336.5:n.428T>A
|
|
|
ENST00000481169.5:c.1865-1097T>A
|
ENSP00000418773.1:n.1865-1097T>A
|
|
ENST00000489736.5:n.1279T>A
|
|
|
ENST00000490639.5:n.2086T>A
|
|
|
ENST00000494544.1:c.1403T>A
|
ENSP00000420545.1:p.Leu468His
|
|
ENST00000497902.5:n.235T>A
|
|
|
NM_000096.3:c.2054T>A
|
NP_000087.1:p.Leu685His
|
|
NR_046371.1:n.2118-1097T>A
|
|
|
XM_006713499.2:c.2054T>A
|
XP_006713562.1:p.Leu685His
|
|
XM_006713500.2:c.2054T>A
|
XP_006713563.1:p.Leu685His
|
|
XM_006713501.2:c.2054T>A
|
XP_006713564.1:p.Leu685His
|
|
XM_006713502.2:c.2054T>A
|
XP_006713565.1:p.Leu685His
|
|
XM_011512435.1:c.2054T>A
|
XP_011510737.1:p.Leu685His
|
|
XR_427361.2:n.2312T>A
|
|
|
XM_006713499.3:c.2054T>A
|
XP_006713562.1:p.Leu685His
|
|
XM_006713500.4:c.2054T>A
|
XP_006713563.1:p.Leu685His
|
|
XM_006713501.3:c.2054T>A
|
XP_006713564.1:p.Leu685His
|
|
XM_011512435.2:c.2054T>A
|
XP_011510737.1:p.Leu685His
|
|
XM_017005734.2:c.2054T>A
|
XP_016861223.1:p.Leu685His
|
|
XM_017005735.2:c.2054T>A
|
XP_016861224.1:p.Leu685His
|
|
XR_427361.3:n.2270T>A
|
|
|
NM_000096.4:c.2054T>A
MANE Select
|
NP_000087.2:p.Leu685His
|
|
NR_046371.2:n.1902-1097T>A
|
|
|