ENST00000356839.10:c.721T>C
MANE Select
|
ENSP00000349297.5:p.Tyr241His
|
|
ENST00000322910.9:c.*676T>C
|
ENSP00000325395.5:n.*676T>C
|
|
ENST00000350303.9:c.655T>C
|
ENSP00000344152.5:p.Tyr219His
|
|
ENST00000356839.9:c.721T>C
|
ENSP00000349297.5:p.Tyr241His
|
|
ENST00000543245.6:c.790T>C
|
ENSP00000438689.2:p.Tyr264His
|
|
ENST00000577191.5:n.798T>C
|
|
|
ENST00000577857.5:n.537T>C
|
|
|
ENST00000579286.5:n.902T>C
|
|
|
ENST00000580365.1:n.452T>C
|
|
|
ENST00000581378.5:c.439T>C
|
|
|
ENST00000582379.1:n.105T>C
|
|
|
ENST00000583760.1:n.503T>C
|
|
|
NM_000018.3:c.721T>C
|
NP_000009.1:p.Tyr241His
|
|
NM_001033859.2:c.655T>C
|
NP_001029031.1:p.Tyr219His
|
|
NM_001270447.1:c.790T>C
|
NP_001257376.1:p.Tyr264His
|
|
NM_001270448.1:c.493T>C
|
NP_001257377.1:p.Tyr165His
|
|
XM_006721516.2:c.721T>C
|
XP_006721579.2:p.Tyr241His
|
|
XM_011523829.1:c.721T>C
|
XP_011522131.1:p.Tyr241His
|
|
XM_011523830.1:c.721T>C
|
XP_011522132.1:p.Tyr241His
|
|
XR_934021.1:n.828T>C
|
|
|
XR_934022.1:n.828T>C
|
|
|
XR_934023.1:n.828T>C
|
|
|
XM_006721516.3:c.721T>C
|
XP_006721579.2:p.Tyr241His
|
|
XM_011523829.2:c.721T>C
|
XP_011522131.1:p.Tyr241His
|
|
XM_011523830.2:c.721T>C
|
XP_011522132.1:p.Tyr241His
|
|
XM_024450741.1:c.721T>C
|
XP_024306509.1:p.Tyr241His
|
|
XR_934021.2:n.780T>C
|
|
|
XR_934022.2:n.780T>C
|
|
|
XR_934023.2:n.780T>C
|
|
|
NM_000018.4:c.721T>C
MANE Select
|
NP_000009.1:p.Tyr241His
|
|
NM_001033859.3:c.655T>C
|
NP_001029031.1:p.Tyr219His
|
|
NM_001270447.2:c.790T>C
|
NP_001257376.1:p.Tyr264His
|
|
NM_001270448.2:c.493T>C
|
NP_001257377.1:p.Tyr165His
|
|