|
ENST00000356839.10:c.935T>C
MANE Select
|
ENSP00000349297.5:p.Phe312Ser
|
|
|
ENST00000322910.9:c.*890T>C
|
ENSP00000325395.5:n.*890T>C
|
|
|
ENST00000350303.9:c.869T>C
|
ENSP00000344152.5:p.Phe290Ser
|
|
|
ENST00000356839.9:c.935T>C
|
ENSP00000349297.5:p.Phe312Ser
|
|
|
ENST00000543245.6:c.1004T>C
|
ENSP00000438689.2:p.Phe335Ser
|
|
|
ENST00000578824.5:n.84T>C
|
|
|
|
ENST00000581378.5:c.653T>C
|
|
|
|
ENST00000582379.1:n.319T>C
|
|
|
|
NM_000018.3:c.935T>C
|
NP_000009.1:p.Phe312Ser
|
|
|
NM_001033859.2:c.869T>C
|
NP_001029031.1:p.Phe290Ser
|
|
|
NM_001270447.1:c.1004T>C
|
NP_001257376.1:p.Phe335Ser
|
|
|
NM_001270448.1:c.707T>C
|
NP_001257377.1:p.Phe236Ser
|
|
|
XM_006721516.2:c.935T>C
|
XP_006721579.2:p.Phe312Ser
|
|
|
XM_011523829.1:c.935T>C
|
XP_011522131.1:p.Phe312Ser
|
|
|
XM_011523830.1:c.935T>C
|
XP_011522132.1:p.Phe312Ser
|
|
|
XR_934021.1:n.1042T>C
|
|
|
|
XR_934022.1:n.1042T>C
|
|
|
|
XR_934023.1:n.1042T>C
|
|
|
|
XM_006721516.3:c.935T>C
|
XP_006721579.2:p.Phe312Ser
|
|
|
XM_011523829.2:c.935T>C
|
XP_011522131.1:p.Phe312Ser
|
|
|
XM_011523830.2:c.935T>C
|
XP_011522132.1:p.Phe312Ser
|
|
|
XM_024450741.1:c.935T>C
|
XP_024306509.1:p.Phe312Ser
|
|
|
XR_934021.2:n.994T>C
|
|
|
|
XR_934022.2:n.994T>C
|
|
|
|
XR_934023.2:n.994T>C
|
|
|
|
NM_000018.4:c.935T>C
MANE Select
|
NP_000009.1:p.Phe312Ser
|
|
|
NM_001033859.3:c.869T>C
|
NP_001029031.1:p.Phe290Ser
|
|
|
NM_001270447.2:c.1004T>C
|
NP_001257376.1:p.Phe335Ser
|
|
|
NM_001270448.2:c.707T>C
|
NP_001257377.1:p.Phe236Ser
|
|
