ENST00000247933.9:c.1291G>T
|
ENSP00000247933.4:p.Ala431Ser
|
|
ENST00000514224.2:c.1291G>T
MANE Select
|
ENSP00000425081.2:p.Ala431Ser
|
|
ENST00000652070.1:n.1347G>T
|
|
|
ENST00000247933.8:c.1291G>T
|
ENSP00000247933.4:p.Ala431Ser
|
|
ENST00000502829.1:n.93G>T
|
|
|
ENST00000514224.1:c.895G>T
|
ENSP00000425081.1:p.Ala299Ser
|
|
ENST00000514698.5:n.1398G>T
|
|
|
NM_000203.4:c.1291G>T
|
NP_000194.2:p.Ala431Ser
|
|
NR_110313.1:n.1379G>T
|
|
|
XM_006713882.2:c.895G>T
|
XP_006713945.1:p.Ala299Ser
|
|
XM_011513459.1:c.1357G>T
|
XP_011511761.1:p.Ala453Ser
|
|
XM_011513460.1:c.1150G>T
|
XP_011511762.1:p.Ala384Ser
|
|
XM_011513461.1:c.1084G>T
|
XP_011511763.1:p.Ala362Ser
|
|
XM_011513462.1:c.1003G>T
|
XP_011511764.1:p.Ala335Ser
|
|
XM_011513463.1:c.1003G>T
|
XP_011511765.1:p.Ala335Ser
|
|
XR_924947.1:n.1360G>T
|
|
|
NM_000203.5:c.1291G>T
MANE Select
|
NP_000194.2:p.Ala431Ser
|
|
NM_001363576.1:c.895G>T
|
NP_001350505.1:p.Ala299Ser
|
|
XM_011513461.2:c.1084G>T
|
XP_011511763.1:p.Ala362Ser
|
|
XM_017008163.1:c.331G>T
|
XP_016863652.1:p.Ala111Ser
|
|