ENST00000247933.9:c.1557C>G
|
ENSP00000247933.4:p.Pro519=
|
|
ENST00000514224.2:c.1557C>G
MANE Select
|
ENSP00000425081.2:p.Pro519=
|
|
ENST00000652070.1:n.1613C>G
|
|
|
ENST00000247933.8:c.1557C>G
|
ENSP00000247933.4:p.Pro519=
|
|
ENST00000502829.1:n.546C>G
|
|
|
ENST00000514224.1:c.1161C>G
|
ENSP00000425081.1:p.Pro387=
|
|
ENST00000514698.5:n.1664C>G
|
|
|
NM_000203.4:c.1557C>G
|
NP_000194.2:p.Pro519=
|
|
NR_110313.1:n.1645C>G
|
|
|
XM_006713882.2:c.1161C>G
|
XP_006713945.1:p.Pro387=
|
|
XM_011513459.1:c.1623C>G
|
XP_011511761.1:p.Pro541=
|
|
XM_011513460.1:c.1416C>G
|
XP_011511762.1:p.Pro472=
|
|
XM_011513461.1:c.1350C>G
|
XP_011511763.1:p.Pro450=
|
|
XM_011513462.1:c.1269C>G
|
XP_011511764.1:p.Pro423=
|
|
XM_011513463.1:c.1269C>G
|
XP_011511765.1:p.Pro423=
|
|
XR_924947.1:n.1813C>G
|
|
|
NM_000203.5:c.1557C>G
MANE Select
|
NP_000194.2:p.Pro519=
|
|
NM_001363576.1:c.1161C>G
|
NP_001350505.1:p.Pro387=
|
|
XM_011513461.2:c.1350C>G
|
XP_011511763.1:p.Pro450=
|
|
XM_017008163.1:c.597C>G
|
XP_016863652.1:p.Pro199=
|
|