ENST00000281928.9:c.4340T>C
MANE Select
|
ENSP00000281928.3:p.Met1447Thr
|
|
ENST00000549786.2:c.3768T>C
|
|
|
ENST00000648379.1:n.2708T>C
|
|
|
ENST00000648737.1:n.4104T>C
|
|
|
ENST00000648825.1:n.1080T>C
|
|
|
ENST00000648916.1:n.2351T>C
|
|
|
ENST00000649146.1:n.1070T>C
|
|
|
ENST00000649607.1:c.2524T>C
|
|
|
ENST00000649775.1:c.837T>C
|
|
|
ENST00000650091.1:n.2316T>C
|
|
|
ENST00000650226.1:c.4340T>C
|
ENSP00000496981.1:p.Met1447Thr
|
|
ENST00000281928.7:c.4340T>C
|
ENSP00000281928.3:p.Met1447Thr
|
|
NM_015335.4:c.4340T>C
|
NP_056150.1:p.Met1447Thr
|
|
XM_011538080.1:c.4340T>C
|
XP_011536382.1:p.Met1447Thr
|
|
XM_011538081.1:c.4337T>C
|
XP_011536383.1:p.Met1446Thr
|
|
XM_011538082.1:c.4310T>C
|
XP_011536384.1:p.Met1437Thr
|
|
XM_011538080.2:c.4340T>C
|
XP_011536382.1:p.Met1447Thr
|
|
XM_011538081.2:c.4337T>C
|
XP_011536383.1:p.Met1446Thr
|
|
XM_011538082.2:c.4310T>C
|
XP_011536384.1:p.Met1437Thr
|
|
XM_017019090.1:c.4337T>C
|
XP_016874579.1:p.Met1446Thr
|
|
NM_015335.5:c.4340T>C
MANE Select
|
NP_056150.1:p.Met1447Thr
|
|