ENST00000356839.10:c.312G>C
MANE Select
|
ENSP00000349297.5:p.Glu104Asp
|
|
ENST00000322910.9:c.*267G>C
|
ENSP00000325395.5:n.*267G>C
|
|
ENST00000350303.9:c.246G>C
|
ENSP00000344152.5:p.Glu82Asp
|
|
ENST00000356839.9:c.312G>C
|
ENSP00000349297.5:p.Glu104Asp
|
|
ENST00000543245.6:c.381G>C
|
ENSP00000438689.2:p.Glu127Asp
|
|
ENST00000577191.5:n.389G>C
|
|
|
ENST00000577433.5:n.520G>C
|
|
|
ENST00000577857.5:n.263G>C
|
|
|
ENST00000579286.5:n.493G>C
|
|
|
ENST00000579886.2:c.202-145G>C
|
ENSP00000463246.1:n.202-145G>C
|
|
ENST00000580365.1:n.43G>C
|
|
|
ENST00000581378.5:c.11G>C
|
|
|
ENST00000581562.5:n.359G>C
|
|
|
ENST00000582056.5:n.402G>C
|
|
|
ENST00000582166.1:n.200G>C
|
|
|
ENST00000582356.5:n.511G>C
|
|
|
ENST00000583312.5:c.312G>C
|
ENSP00000467920.1:p.Glu104Asp
|
|
ENST00000584103.5:c.312G>C
|
ENSP00000465353.1:p.Glu104Asp
|
|
NM_000018.3:c.312G>C
|
NP_000009.1:p.Glu104Asp
|
|
NM_001033859.2:c.246G>C
|
NP_001029031.1:p.Glu82Asp
|
|
NM_001270447.1:c.381G>C
|
NP_001257376.1:p.Glu127Asp
|
|
NM_001270448.1:c.84G>C
|
NP_001257377.1:p.Glu28Asp
|
|
XM_006721516.2:c.312G>C
|
XP_006721579.2:p.Glu104Asp
|
|
XM_011523829.1:c.312G>C
|
XP_011522131.1:p.Glu104Asp
|
|
XM_011523830.1:c.312G>C
|
XP_011522132.1:p.Glu104Asp
|
|
XR_934021.1:n.419G>C
|
|
|
XR_934022.1:n.419G>C
|
|
|
XR_934023.1:n.419G>C
|
|
|
XM_006721516.3:c.312G>C
|
XP_006721579.2:p.Glu104Asp
|
|
XM_011523829.2:c.312G>C
|
XP_011522131.1:p.Glu104Asp
|
|
XM_011523830.2:c.312G>C
|
XP_011522132.1:p.Glu104Asp
|
|
XM_024450741.1:c.312G>C
|
XP_024306509.1:p.Glu104Asp
|
|
XR_934021.2:n.371G>C
|
|
|
XR_934022.2:n.371G>C
|
|
|
XR_934023.2:n.371G>C
|
|
|
NM_000018.4:c.312G>C
MANE Select
|
NP_000009.1:p.Glu104Asp
|
|
NM_001033859.3:c.246G>C
|
NP_001029031.1:p.Glu82Asp
|
|
NM_001270447.2:c.381G>C
|
NP_001257376.1:p.Glu127Asp
|
|
NM_001270448.2:c.84G>C
|
NP_001257377.1:p.Glu28Asp
|
|