ENST00000225927.7:c.1833T>C
MANE Select
|
ENSP00000225927.1:p.Ala611=
|
|
ENST00000225927.6:c.1833T>C
|
ENSP00000225927.1:p.Ala611=
|
|
ENST00000591587.1:c.1171T>C
|
ENSP00000467836.1:n.1171T>C
|
|
NM_000263.3:c.1833T>C
|
NP_000254.2:p.Ala611=
|
|
XM_006721920.2:c.1002T>C
|
XP_006721983.1:p.Ala334=
|
|
XM_011524840.1:c.834T>C
|
XP_011523142.1:p.Ala278=
|
|
XM_017024687.1:c.1002T>C
|
XP_016880176.1:p.Ala334=
|
|
XM_024450771.1:c.1890T>C
|
XP_024306539.1:p.Ala630=
|
|
XM_024450772.1:c.834T>C
|
XP_024306540.1:p.Ala278=
|
|
NM_000263.4:c.1833T>C
MANE Select
|
NP_000254.2:p.Ala611=
|
|