ENST00000261937.11:c.4081A>C
MANE Select
|
ENSP00000261937.6:p.Asn1361His
|
|
ENST00000261937.10:c.4081A>C
|
ENSP00000261937.6:p.Asn1361His
|
|
ENST00000502603.5:n.781A>C
|
|
|
NM_182925.4:c.4081A>C
|
NP_891555.2:p.Asn1361His
|
|
XM_011534477.1:c.4330A>C
|
XP_011532779.1:p.Asn1444His
|
|
XM_011534478.1:c.4312A>C
|
XP_011532780.1:p.Asn1438His
|
|
XM_011534482.1:c.4099A>C
|
XP_011532784.1:p.Asn1367His
|
|
XM_011534483.1:c.4021A>C
|
XP_011532785.1:p.Asn1341His
|
|
XM_011534484.1:c.3622A>C
|
XP_011532786.1:p.Asn1208His
|
|
XR_941095.1:n.4367A>C
|
|
|
XM_011534478.3:c.4312A>C
|
XP_011532780.1:p.Asn1438His
|
|
XM_011534484.2:c.3622A>C
|
XP_011532786.1:p.Asn1208His
|
|
XM_017009263.1:c.*227A>C
|
XP_016864752.1:n.*227A>C
|
|
XM_017009268.1:c.4003A>C
|
XP_016864757.1:p.Asn1335His
|
|
XR_001742050.2:n.4571A>C
|
|
|
NM_182925.5:c.4081A>C
MANE Select
|
NP_891555.2:p.Asn1361His
|
|