ENST00000372563.2:c.1055A>C
MANE Select
|
ENSP00000361644.1:p.Lys352Thr
|
|
ENST00000327674.8:c.1055A>C
|
ENSP00000329374.4:p.Lys352Thr
|
|
ENST00000372563.1:c.1055A>C
|
ENSP00000361644.1:p.Lys352Thr
|
|
ENST00000487487.1:n.389A>C
|
|
|
NM_000354.5:c.1055A>C
|
NP_000345.2:p.Lys352Thr
|
|
XM_005262180.3:c.1116A>C
|
XP_005262237.1:p.Ter372Tyr
|
|
XM_006724683.1:c.1085A>C
|
XP_006724746.1:p.Lys362Thr
|
|
XM_005262180.4:c.1116A>C
|
XP_005262237.1:p.Ter372Tyr
|
|
XM_006724683.2:c.1085A>C
|
XP_006724746.1:p.Lys362Thr
|
|
NM_000354.6:c.1055A>C
MANE Select
|
NP_000345.2:p.Lys352Thr
|
|