ENST00000341459.8:c.346G>T
MANE Select
|
ENSP00000341550.3:p.Ala116Ser
|
|
ENST00000341459.7:c.346G>T
|
ENSP00000341550.3:p.Ala116Ser
|
|
ENST00000449382.2:c.166G>T
|
ENSP00000389966.2:p.Ala56Ser
|
|
ENST00000463289.1:n.106G>T
|
|
|
NM_205850.2:c.346G>T
|
NP_995322.1:p.Ala116Ser
|
|
XM_011521458.1:c.346G>T
|
XP_011519760.1:p.Ala116Ser
|
|
XM_017022079.1:c.7G>T
|
XP_016877568.1:p.Ala3Ser
|
|
XM_017022080.1:c.7G>T
|
XP_016877569.1:p.Ala3Ser
|
|
XM_024449901.1:c.7G>T
|
XP_024305669.1:p.Ala3Ser
|
|
NM_205850.3:c.346G>T
MANE Select
|
NP_995322.1:p.Ala116Ser
|
|