ENST00000285968.11:c.5632C>A
MANE Select
|
ENSP00000285968.6:p.Arg1878Ser
|
|
ENST00000285968.10:c.5632C>A
|
ENSP00000285968.6:p.Arg1878Ser
|
|
ENST00000461255.5:n.839C>A
|
|
|
ENST00000477620.5:c.1394C>A
|
|
|
ENST00000490439.1:c.69C>A
|
|
|
ENST00000607647.5:n.3910C>A
|
|
|
NM_015135.2:c.5632C>A
|
NP_055950.1:p.Arg1878Ser
|
|
XM_005250235.2:c.4558C>A
|
XP_005250292.1:p.Arg1520Ser
|
|
NM_001329434.1:c.4558C>A
|
NP_001316363.1:p.Arg1520Ser
|
|
NM_015135.3:c.5632C>A
MANE Select
|
NP_055950.2:p.Arg1878Ser
|
|
NM_001329434.2:c.4558C>A
|
NP_001316363.2:p.Arg1520Ser
|
|