|
ENST00000356839.10:c.1557G=
MANE Select
|
ENSP00000349297.5:p.Leu519=
|
|
|
ENST00000322910.9:c.*1512G=
|
ENSP00000325395.5:n.*1512G=
|
|
|
ENST00000350303.9:c.1491G=
|
ENSP00000344152.5:p.Leu497=
|
|
|
ENST00000356839.9:c.1557G=
|
ENSP00000349297.5:p.Leu519=
|
|
|
ENST00000542255.6:c.415G=
|
|
|
|
ENST00000543245.6:c.1626G=
|
ENSP00000438689.2:p.Leu542=
|
|
|
ENST00000578319.5:n.52G=
|
|
|
|
ENST00000578711.1:n.841G=
|
|
|
|
ENST00000578809.5:n.129G=
|
|
|
|
ENST00000579391.1:n.165G=
|
|
|
|
ENST00000579425.5:n.673G=
|
|
|
|
ENST00000579546.1:c.296G=
|
|
|
|
ENST00000579894.5:n.344G=
|
|
|
|
ENST00000582450.1:n.65G=
|
|
|
|
ENST00000583074.5:n.178G=
|
|
|
|
ENST00000583850.5:n.332G=
|
|
|
|
ENST00000583858.5:c.488G=
|
|
|
|
ENST00000585203.6:n.748G=
|
|
|
|
NM_000018.3:c.1557G=
|
NP_000009.1:p.Leu519=
|
|
|
NM_001033859.2:c.1491G=
|
NP_001029031.1:p.Leu497=
|
|
|
NM_001270447.1:c.1626G=
|
NP_001257376.1:p.Leu542=
|
|
|
NM_001270448.1:c.1329G=
|
NP_001257377.1:p.Leu443=
|
|
|
XM_006721516.2:c.1557G=
|
XP_006721579.2:p.Leu519=
|
|
|
XM_011523829.1:c.1459G=
|
XP_011522131.1:p.Glu487=
|
|
|
XM_011523830.1:c.1459G=
|
XP_011522132.1:p.Glu487=
|
|
|
XR_934021.1:n.1664G=
|
|
|
|
XR_934022.1:n.1566G=
|
|
|
|
XR_934023.1:n.1566G=
|
|
|
|
XM_006721516.3:c.1557G=
|
XP_006721579.2:p.Leu519=
|
|
|
XM_011523829.2:c.1459G=
|
XP_011522131.1:p.Glu487=
|
|
|
XM_011523830.2:c.1459G=
|
XP_011522132.1:p.Glu487=
|
|
|
XM_024450741.1:c.1459G=
|
XP_024306509.1:p.Glu487=
|
|
|
XR_934021.2:n.1616G=
|
|
|
|
XR_934022.2:n.1518G=
|
|
|
|
XR_934023.2:n.1518G=
|
|
|
|
NM_000018.4:c.1557G=
MANE Select
|
NP_000009.1:p.Leu519=
|
|
|
NM_001033859.3:c.1491G=
|
NP_001029031.1:p.Leu497=
|
|
|
NM_001270447.2:c.1626G=
|
NP_001257376.1:p.Leu542=
|
|
|
NM_001270448.2:c.1329G=
|
NP_001257377.1:p.Leu443=
|
|
