ENST00000356839.10:c.1820G>C
MANE Select
|
ENSP00000349297.5:p.Cys607Ser
|
|
ENST00000322910.9:c.*1775G>C
|
ENSP00000325395.5:n.*1775G>C
|
|
ENST00000350303.9:c.1754G>C
|
ENSP00000344152.5:p.Cys585Ser
|
|
ENST00000356839.9:c.1820G>C
|
ENSP00000349297.5:p.Cys607Ser
|
|
ENST00000542255.6:c.699G>C
|
|
|
ENST00000543245.6:c.1889G>C
|
ENSP00000438689.2:p.Cys630Ser
|
|
ENST00000578033.1:n.245G>C
|
|
|
ENST00000578319.5:n.401G>C
|
|
|
ENST00000578711.1:n.1373G>C
|
|
|
ENST00000578809.5:n.392G>C
|
|
|
ENST00000579425.5:n.936G>C
|
|
|
ENST00000579546.1:c.555G>C
|
|
|
ENST00000583848.5:c.186G>C
|
ENSP00000466487.1:n.186G>C
|
|
ENST00000583850.5:n.591G>C
|
|
|
ENST00000583858.5:c.751G>C
|
|
|
NM_000018.3:c.1820G>C
|
NP_000009.1:p.Cys607Ser
|
|
NM_001033859.2:c.1754G>C
|
NP_001029031.1:p.Cys585Ser
|
|
NM_001270447.1:c.1889G>C
|
NP_001257376.1:p.Cys630Ser
|
|
NM_001270448.1:c.1592G>C
|
NP_001257377.1:p.Cys531Ser
|
|
XM_006721516.2:c.1841G>C
|
XP_006721579.2:p.Cys614Ser
|
|
XM_011523829.1:c.1739G>C
|
XP_011522131.1:p.Cys580Ser
|
|
XM_011523830.1:c.1718G>C
|
XP_011522132.1:p.Cys573Ser
|
|
XR_934021.1:n.1923G>C
|
|
|
XR_934022.1:n.1829G>C
|
|
|
XR_934023.1:n.1850G>C
|
|
|
XM_006721516.3:c.1841G>C
|
XP_006721579.2:p.Cys614Ser
|
|
XM_011523829.2:c.1739G>C
|
XP_011522131.1:p.Cys580Ser
|
|
XM_011523830.2:c.1718G>C
|
XP_011522132.1:p.Cys573Ser
|
|
XM_024450741.1:c.1808G>C
|
XP_024306509.1:p.Cys603Ser
|
|
XR_934021.2:n.1875G>C
|
|
|
XR_934022.2:n.1781G>C
|
|
|
XR_934023.2:n.1802G>C
|
|
|
NM_000018.4:c.1820G>C
MANE Select
|
NP_000009.1:p.Cys607Ser
|
|
NM_001033859.3:c.1754G>C
|
NP_001029031.1:p.Cys585Ser
|
|
NM_001270447.2:c.1889G>C
|
NP_001257376.1:p.Cys630Ser
|
|
NM_001270448.2:c.1592G>C
|
NP_001257377.1:p.Cys531Ser
|
|