|
ENST00000356839.10:c.1183-79T>G
MANE Select
|
ENSP00000349297.5:n.1183-79T>G
|
|
|
ENST00000322910.9:c.*1138-79T>G
|
ENSP00000325395.5:n.*1138-79T>G
|
|
|
ENST00000350303.9:c.1117-79T>G
|
ENSP00000344152.5:n.1117-79T>G
|
|
|
ENST00000356839.9:c.1183-79T>G
|
ENSP00000349297.5:n.1183-79T>G
|
|
|
ENST00000542255.6:c.41-79T>G
|
|
|
|
ENST00000543245.6:c.1252-79T>G
|
ENSP00000438689.2:n.1252-79T>G
|
|
|
ENST00000578579.2:n.275T>G
|
|
|
|
ENST00000578711.1:n.61T>G
|
|
|
|
ENST00000578824.5:n.599-79T>G
|
|
|
|
ENST00000579425.5:n.207-79T>G
|
|
|
|
ENST00000579546.1:c.20-79T>G
|
|
|
|
ENST00000583858.5:c.212-79T>G
|
|
|
|
ENST00000585203.6:n.391-79T>G
|
|
|
|
NM_000018.3:c.1183-79T>G
|
NP_000009.1:n.1183-79T>G
|
|
|
NM_001033859.2:c.1117-79T>G
|
NP_001029031.1:n.1117-79T>G
|
|
|
NM_001270447.1:c.1252-79T>G
|
NP_001257376.1:n.1252-79T>G
|
|
|
NM_001270448.1:c.955-79T>G
|
NP_001257377.1:n.955-79T>G
|
|
|
XM_006721516.2:c.1183-79T>G
|
XP_006721579.2:n.1183-79T>G
|
|
|
XM_011523829.1:c.1183-79T>G
|
XP_011522131.1:n.1183-79T>G
|
|
|
XM_011523830.1:c.1183-79T>G
|
XP_011522132.1:n.1183-79T>G
|
|
|
XR_934021.1:n.1290-79T>G
|
|
|
|
XR_934022.1:n.1290-79T>G
|
|
|
|
XR_934023.1:n.1290-79T>G
|
|
|
|
XM_006721516.3:c.1183-79T>G
|
XP_006721579.2:n.1183-79T>G
|
|
|
XM_011523829.2:c.1183-79T>G
|
XP_011522131.1:n.1183-79T>G
|
|
|
XM_011523830.2:c.1183-79T>G
|
XP_011522132.1:n.1183-79T>G
|
|
|
XM_024450741.1:c.1183-79T>G
|
XP_024306509.1:n.1183-79T>G
|
|
|
XR_934021.2:n.1242-79T>G
|
|
|
|
XR_934022.2:n.1242-79T>G
|
|
|
|
XR_934023.2:n.1242-79T>G
|
|
|
|
NM_000018.4:c.1183-79T>G
MANE Select
|
NP_000009.1:n.1183-79T>G
|
|
|
NM_001033859.3:c.1117-79T>G
|
NP_001029031.1:n.1117-79T>G
|
|
|
NM_001270447.2:c.1252-79T>G
|
NP_001257376.1:n.1252-79T>G
|
|
|
NM_001270448.2:c.955-79T>G
|
NP_001257377.1:n.955-79T>G
|
|
