ENST00000258530.8:c.1453G>T
MANE Select
|
ENSP00000258530.3:p.Ala485Ser
|
|
ENST00000258530.7:c.1453G>T
|
ENSP00000258530.3:p.Ala485Ser
|
|
ENST00000539978.6:c.1324G>T
|
ENSP00000444472.2:p.Ala442Ser
|
|
ENST00000547439.5:c.*738G>T
|
ENSP00000449410.1:n.*738G>T
|
|
ENST00000547809.5:n.1463G>T
|
|
|
ENST00000551662.5:c.1471G>T
|
ENSP00000446917.1:p.Ala491Ser
|
|
ENST00000552945.1:n.293G>T
|
|
|
ENST00000553109.1:c.97G>T
|
ENSP00000446510.1:p.Ala33Ser
|
|
NM_001251904.1:c.1471G>T
|
NP_001238833.1:p.Ala491Ser
|
|
NM_001251905.1:c.1324G>T
|
NP_001238834.1:p.Ala442Ser
|
|
NM_018171.3:c.1453G>T
|
NP_060641.2:p.Ala485Ser
|
|
XM_006719472.1:c.1471G>T
|
XP_006719535.1:p.Ala491Ser
|
|
XM_011538530.1:c.1432G>T
|
XP_011536832.1:p.Ala478Ser
|
|
XM_011538531.1:c.1342G>T
|
XP_011536833.1:p.Ala448Ser
|
|
XM_011538532.1:c.1342G>T
|
XP_011536834.1:p.Ala448Ser
|
|
XM_011538530.3:c.1432G>T
|
XP_011536832.1:p.Ala478Ser
|
|
XM_011538531.3:c.1342G>T
|
XP_011536833.1:p.Ala448Ser
|
|
XM_011538532.3:c.1342G>T
|
XP_011536834.1:p.Ala448Ser
|
|
XM_017019551.2:c.1414G>T
|
XP_016875040.1:p.Ala472Ser
|
|
XM_017019552.2:c.1324G>T
|
XP_016875041.1:p.Ala442Ser
|
|
XM_017019553.2:c.1324G>T
|
XP_016875042.1:p.Ala442Ser
|
|
XM_017019554.1:c.1453G>T
|
XP_016875043.1:p.Ala485Ser
|
|
XR_001748795.1:n.1633G>T
|
|
|
XR_001748796.1:n.1615G>T
|
|
|
NM_018171.4:c.1453G>T
|
NP_060641.2:p.Ala485Ser
|
|
NM_018171.5:c.1453G>T
MANE Select
|
NP_060641.2:p.Ala485Ser
|
|
NM_001251904.2:c.1471G>T
|
NP_001238833.1:p.Ala491Ser
|
|
NM_001251905.2:c.1324G>T
|
NP_001238834.1:p.Ala442Ser
|
|