|
ENST00000356839.10:c.1573G>C
MANE Select
|
ENSP00000349297.5:p.Val525Leu
|
|
|
ENST00000322910.9:c.*1528G>C
|
ENSP00000325395.5:n.*1528G>C
|
|
|
ENST00000350303.9:c.1507G>C
|
ENSP00000344152.5:p.Val503Leu
|
|
|
ENST00000356839.9:c.1573G>C
|
ENSP00000349297.5:p.Val525Leu
|
|
|
ENST00000542255.6:c.431G>C
|
|
|
|
ENST00000543245.6:c.1642G>C
|
ENSP00000438689.2:p.Val548Leu
|
|
|
ENST00000578319.5:n.68G>C
|
|
|
|
ENST00000578711.1:n.857G>C
|
|
|
|
ENST00000578809.5:n.145G>C
|
|
|
|
ENST00000579391.1:n.181G>C
|
|
|
|
ENST00000579425.5:n.689G>C
|
|
|
|
ENST00000579546.1:c.312G>C
|
|
|
|
ENST00000579894.5:n.360G>C
|
|
|
|
ENST00000582450.1:n.81G>C
|
|
|
|
ENST00000583074.5:n.194G>C
|
|
|
|
ENST00000583850.5:n.348G>C
|
|
|
|
ENST00000583858.5:c.504G>C
|
|
|
|
ENST00000585203.6:n.764G>C
|
|
|
|
NM_000018.3:c.1573G>C
|
NP_000009.1:p.Val525Leu
|
|
|
NM_001033859.2:c.1507G>C
|
NP_001029031.1:p.Val503Leu
|
|
|
NM_001270447.1:c.1642G>C
|
NP_001257376.1:p.Val548Leu
|
|
|
NM_001270448.1:c.1345G>C
|
NP_001257377.1:p.Val449Leu
|
|
|
XM_006721516.2:c.1573G>C
|
XP_006721579.2:p.Val525Leu
|
|
|
XM_011523829.1:c.1475G>C
|
XP_011522131.1:p.Cys492Ser
|
|
|
XM_011523830.1:c.1475G>C
|
XP_011522132.1:p.Cys492Ser
|
|
|
XR_934021.1:n.1680G>C
|
|
|
|
XR_934022.1:n.1582G>C
|
|
|
|
XR_934023.1:n.1582G>C
|
|
|
|
XM_006721516.3:c.1573G>C
|
XP_006721579.2:p.Val525Leu
|
|
|
XM_011523829.2:c.1475G>C
|
XP_011522131.1:p.Cys492Ser
|
|
|
XM_011523830.2:c.1475G>C
|
XP_011522132.1:p.Cys492Ser
|
|
|
XM_024450741.1:c.1475G>C
|
XP_024306509.1:p.Cys492Ser
|
|
|
XR_934021.2:n.1632G>C
|
|
|
|
XR_934022.2:n.1534G>C
|
|
|
|
XR_934023.2:n.1534G>C
|
|
|
|
NM_000018.4:c.1573G>C
MANE Select
|
NP_000009.1:p.Val525Leu
|
|
|
NM_001033859.3:c.1507G>C
|
NP_001029031.1:p.Val503Leu
|
|
|
NM_001270447.2:c.1642G>C
|
NP_001257376.1:p.Val548Leu
|
|
|
NM_001270448.2:c.1345G>C
|
NP_001257377.1:p.Val449Leu
|
|
