|
ENST00000356839.10:c.1320G>C
MANE Select
|
ENSP00000349297.5:p.Met440Ile
|
|
|
ENST00000322910.9:c.*1275G>C
|
ENSP00000325395.5:n.*1275G>C
|
|
|
ENST00000350303.9:c.1254G>C
|
ENSP00000344152.5:p.Met418Ile
|
|
|
ENST00000356839.9:c.1320G>C
|
ENSP00000349297.5:p.Met440Ile
|
|
|
ENST00000542255.6:c.178G>C
|
|
|
|
ENST00000543245.6:c.1389G>C
|
ENSP00000438689.2:p.Met463Ile
|
|
|
ENST00000578711.1:n.359G>C
|
|
|
|
ENST00000579425.5:n.344G>C
|
|
|
|
ENST00000579546.1:c.157G>C
|
|
|
|
ENST00000583074.5:n.39G>C
|
|
|
|
ENST00000583850.5:n.95G>C
|
|
|
|
ENST00000583858.5:c.349G>C
|
|
|
|
ENST00000585203.6:n.523+5G>C
|
|
|
|
NM_000018.3:c.1320G>C
|
NP_000009.1:p.Met440Ile
|
|
|
NM_001033859.2:c.1254G>C
|
NP_001029031.1:p.Met418Ile
|
|
|
NM_001270447.1:c.1389G>C
|
NP_001257376.1:p.Met463Ile
|
|
|
NM_001270448.1:c.1092G>C
|
NP_001257377.1:p.Met364Ile
|
|
|
XM_006721516.2:c.1320G>C
|
XP_006721579.2:p.Met440Ile
|
|
|
XM_011523829.1:c.1320G>C
|
XP_011522131.1:p.Met440Ile
|
|
|
XM_011523830.1:c.1320G>C
|
XP_011522132.1:p.Met440Ile
|
|
|
XR_934021.1:n.1427G>C
|
|
|
|
XR_934022.1:n.1427G>C
|
|
|
|
XR_934023.1:n.1427G>C
|
|
|
|
XM_006721516.3:c.1320G>C
|
XP_006721579.2:p.Met440Ile
|
|
|
XM_011523829.2:c.1320G>C
|
XP_011522131.1:p.Met440Ile
|
|
|
XM_011523830.2:c.1320G>C
|
XP_011522132.1:p.Met440Ile
|
|
|
XM_024450741.1:c.1320G>C
|
XP_024306509.1:p.Met440Ile
|
|
|
XR_934021.2:n.1379G>C
|
|
|
|
XR_934022.2:n.1379G>C
|
|
|
|
XR_934023.2:n.1379G>C
|
|
|
|
NM_000018.4:c.1320G>C
MANE Select
|
NP_000009.1:p.Met440Ile
|
|
|
NM_001033859.3:c.1254G>C
|
NP_001029031.1:p.Met418Ile
|
|
|
NM_001270447.2:c.1389G>C
|
NP_001257376.1:p.Met463Ile
|
|
|
NM_001270448.2:c.1092G>C
|
NP_001257377.1:p.Met364Ile
|
|
