ENST00000330342.8:c.736C>A
MANE Select
|
ENSP00000332247.2:p.His246Asn
|
|
ENST00000540368.6:n.767C>A
|
|
|
ENST00000613625.5:c.736C>A
|
ENSP00000482236.1:p.His246Asn
|
|
ENST00000674794.1:c.176C>A
|
|
|
ENST00000675344.1:c.736C>A
|
ENSP00000501953.1:p.His246Asn
|
|
ENST00000330342.7:c.736C>A
|
ENSP00000332247.2:p.His246Asn
|
|
ENST00000504192.2:c.346C>A
|
ENSP00000443441.1:p.His116Asn
|
|
ENST00000540368.5:n.946C>A
|
|
|
ENST00000545059.5:n.3372C>A
|
|
|
ENST00000613625.4:c.736C>A
|
ENSP00000482236.1:p.His246Asn
|
|
NM_012463.3:c.736C>A
|
NP_036595.2:p.His246Asn
|
|
XM_005253563.1:c.736C>A
|
XP_005253620.1:p.His246Asn
|
|
XM_006719317.2:c.223C>A
|
XP_006719380.1:p.His75Asn
|
|
XR_429088.1:n.899C>A
|
|
|
XM_024448910.1:c.736C>A
|
XP_024304678.1:p.His246Asn
|
|
XM_024448911.1:c.223C>A
|
XP_024304679.1:p.His75Asn
|
|
NM_012463.4:c.736C>A
MANE Select
|
NP_036595.2:p.His246Asn
|
|