ENST00000356839.10:c.1328T>C
MANE Select
|
ENSP00000349297.5:p.Met443Thr
|
|
ENST00000322910.9:c.*1283T>C
|
ENSP00000325395.5:n.*1283T>C
|
|
ENST00000350303.9:c.1262T>C
|
ENSP00000344152.5:p.Met421Thr
|
|
ENST00000356839.9:c.1328T>C
|
ENSP00000349297.5:p.Met443Thr
|
|
ENST00000542255.6:c.186T>C
|
|
|
ENST00000543245.6:c.1397T>C
|
ENSP00000438689.2:p.Met466Thr
|
|
ENST00000578711.1:n.367T>C
|
|
|
ENST00000579425.5:n.352T>C
|
|
|
ENST00000579546.1:c.165T>C
|
|
|
ENST00000583074.5:n.47T>C
|
|
|
ENST00000583850.5:n.103T>C
|
|
|
ENST00000583858.5:c.357T>C
|
|
|
ENST00000585203.6:n.523+13T>C
|
|
|
NM_000018.3:c.1328T>C
|
NP_000009.1:p.Met443Thr
|
|
NM_001033859.2:c.1262T>C
|
NP_001029031.1:p.Met421Thr
|
|
NM_001270447.1:c.1397T>C
|
NP_001257376.1:p.Met466Thr
|
|
NM_001270448.1:c.1100T>C
|
NP_001257377.1:p.Met367Thr
|
|
XM_006721516.2:c.1328T>C
|
XP_006721579.2:p.Met443Thr
|
|
XM_011523829.1:c.1328T>C
|
XP_011522131.1:p.Met443Thr
|
|
XM_011523830.1:c.1328T>C
|
XP_011522132.1:p.Met443Thr
|
|
XR_934021.1:n.1435T>C
|
|
|
XR_934022.1:n.1435T>C
|
|
|
XR_934023.1:n.1435T>C
|
|
|
XM_006721516.3:c.1328T>C
|
XP_006721579.2:p.Met443Thr
|
|
XM_011523829.2:c.1328T>C
|
XP_011522131.1:p.Met443Thr
|
|
XM_011523830.2:c.1328T>C
|
XP_011522132.1:p.Met443Thr
|
|
XM_024450741.1:c.1328T>C
|
XP_024306509.1:p.Met443Thr
|
|
XR_934021.2:n.1387T>C
|
|
|
XR_934022.2:n.1387T>C
|
|
|
XR_934023.2:n.1387T>C
|
|
|
NM_000018.4:c.1328T>C
MANE Select
|
NP_000009.1:p.Met443Thr
|
|
NM_001033859.3:c.1262T>C
|
NP_001029031.1:p.Met421Thr
|
|
NM_001270447.2:c.1397T>C
|
NP_001257376.1:p.Met466Thr
|
|
NM_001270448.2:c.1100T>C
|
NP_001257377.1:p.Met367Thr
|
|