ENST00000392334.7:c.176T>C
|
ENSP00000376146.2:p.Met59Thr
|
|
ENST00000314028.11:c.176T>C
MANE Select
|
ENSP00000324464.6:p.Met59Thr
|
|
ENST00000314028.10:c.176T>C
|
ENSP00000324464.6:p.Met59Thr
|
|
ENST00000392334.6:c.176T>C
|
ENSP00000376146.2:p.Met59Thr
|
|
ENST00000398519.9:c.176T>C
|
ENSP00000381531.5:p.Met59Thr
|
|
ENST00000403276.7:c.176T>C
|
ENSP00000385769.3:p.Met59Thr
|
|
ENST00000578194.5:n.382T>C
|
|
|
ENST00000579308.1:n.201T>C
|
|
|
ENST00000579316.5:n.233T>C
|
|
|
ENST00000580061.5:n.176T>C
|
|
|
ENST00000580446.1:c.76+7609T>C
|
ENSP00000463757.1:n.76+7609T>C
|
|
ENST00000581241.5:n.164T>C
|
|
|
ENST00000581660.5:c.*214T>C
|
ENSP00000464551.1:n.*214T>C
|
|
ENST00000582844.5:n.134T>C
|
|
|
ENST00000584472.5:n.261T>C
|
|
|
ENST00000585026.1:c.*222T>C
|
ENSP00000462144.1:n.*222T>C
|
|
NM_001893.4:c.176T>C
|
NP_001884.2:p.Met59Thr
|
|
NM_139062.2:c.176T>C
|
NP_620693.1:p.Met59Thr
|
|
NR_110578.1:n.537T>C
|
|
|
XM_005256336.2:c.176T>C
|
XP_005256393.1:p.Met59Thr
|
|
XM_005256337.3:c.176T>C
|
XP_005256394.1:p.Met59Thr
|
|
XR_243518.2:n.496T>C
|
|
|
XR_430028.2:n.496T>C
|
|
|
XR_933922.1:n.496T>C
|
|
|
XR_933923.1:n.496T>C
|
|
|
NM_001363749.1:c.176T>C
|
NP_001350678.1:p.Met59Thr
|
|
NM_001893.5:c.176T>C
|
NP_001884.2:p.Met59Thr
|
|
NM_139062.3:c.176T>C
|
NP_620693.1:p.Met59Thr
|
|
NR_110578.2:n.545T>C
|
|
|
XM_005256336.4:c.176T>C
|
XP_005256393.1:p.Met59Thr
|
|
XR_002957961.1:n.495T>C
|
|
|
XR_243518.4:n.495T>C
|
|
|
XR_430028.4:n.495T>C
|
|
|
XR_933922.3:n.495T>C
|
|
|
XR_933923.3:n.495T>C
|
|
|
NM_001363749.2:c.176T>C
|
NP_001350678.1:p.Met59Thr
|
|
NM_001893.6:c.176T>C
MANE Select
|
NP_001884.2:p.Met59Thr
|
|
NM_139062.4:c.176T>C
|
NP_620693.1:p.Met59Thr
|
|