ENST00000356839.10:c.1960G>A
MANE Select
|
ENSP00000349297.5:p.Gly654Ser
|
|
ENST00000322910.9:c.*1915G>A
|
ENSP00000325395.5:n.*1915G>A
|
|
ENST00000350303.9:c.1894G>A
|
ENSP00000344152.5:p.Gly632Ser
|
|
ENST00000356839.9:c.1960G>A
|
ENSP00000349297.5:p.Gly654Ser
|
|
ENST00000542255.6:c.839G>A
|
|
|
ENST00000543245.6:c.2029G>A
|
ENSP00000438689.2:p.Gly677Ser
|
|
ENST00000578033.1:n.385G>A
|
|
|
ENST00000578319.5:n.541G>A
|
|
|
ENST00000578711.1:n.1585G>A
|
|
|
ENST00000578809.5:n.532G>A
|
|
|
ENST00000579425.5:n.1076G>A
|
|
|
ENST00000583848.5:c.326G>A
|
ENSP00000466487.1:n.326G>A
|
|
ENST00000583850.5:n.731G>A
|
|
|
ENST00000583858.5:c.891G>A
|
|
|
NM_000018.3:c.1960G>A
|
NP_000009.1:p.Gly654Ser
|
|
NM_001033859.2:c.1894G>A
|
NP_001029031.1:p.Gly632Ser
|
|
NM_001270447.1:c.2029G>A
|
NP_001257376.1:p.Gly677Ser
|
|
NM_001270448.1:c.1732G>A
|
NP_001257377.1:p.Gly578Ser
|
|
XM_006721516.2:c.1981G>A
|
XP_006721579.2:p.Gly661Ser
|
|
XM_011523829.1:c.1879G>A
|
XP_011522131.1:p.Gly627Ser
|
|
XM_011523830.1:c.1858G>A
|
XP_011522132.1:p.Gly620Ser
|
|
XR_934021.1:n.2063G>A
|
|
|
XR_934022.1:n.1969G>A
|
|
|
XR_934023.1:n.1990G>A
|
|
|
XM_006721516.3:c.1981G>A
|
XP_006721579.2:p.Gly661Ser
|
|
XM_011523829.2:c.1879G>A
|
XP_011522131.1:p.Gly627Ser
|
|
XM_011523830.2:c.1858G>A
|
XP_011522132.1:p.Gly620Ser
|
|
XM_024450741.1:c.1948G>A
|
XP_024306509.1:p.Gly650Ser
|
|
XR_934021.2:n.2015G>A
|
|
|
XR_934022.2:n.1921G>A
|
|
|
XR_934023.2:n.1942G>A
|
|
|
NM_000018.4:c.1960G>A
MANE Select
|
NP_000009.1:p.Gly654Ser
|
|
NM_001033859.3:c.1894G>A
|
NP_001029031.1:p.Gly632Ser
|
|
NM_001270447.2:c.2029G>A
|
NP_001257376.1:p.Gly677Ser
|
|
NM_001270448.2:c.1732G>A
|
NP_001257377.1:p.Gly578Ser
|
|