ENST00000650516.2:c.935G=
|
ENSP00000498052.2:p.Ser312=
|
|
ENST00000343257.7:c.935G=
MANE Select
|
ENSP00000339867.2:p.Ser312=
|
|
ENST00000432192.6:c.759G=
|
|
|
ENST00000455478.6:c.523G=
|
ENSP00000400027.2:n.523G=
|
|
ENST00000650516.1:c.935G=
|
ENSP00000498052.1:p.Ser312=
|
|
ENST00000343257.6:c.935G=
|
ENSP00000339867.2:p.Ser312=
|
|
ENST00000432192.5:c.449G=
|
|
|
ENST00000455478.5:c.527G=
|
|
|
ENST00000495612.1:n.236G=
|
|
|
NM_000083.2:c.935G=
|
NP_000074.2:p.Ser312=
|
|
NR_046453.1:n.1025G=
|
|
|
XM_011515781.1:c.935G=
|
XP_011514083.1:p.Ser312=
|
|
XM_017011739.1:c.485G=
|
XP_016867228.1:p.Ser162=
|
|
XM_017011740.1:c.485G=
|
XP_016867229.1:p.Ser162=
|
|
NM_000083.3:c.935G=
MANE Select
|
NP_000074.3:p.Ser312=
|
|
NR_046453.2:n.1040G=
|
|
|