ENST00000650516.2:c.2914G>C
|
ENSP00000498052.2:p.Gly972Arg
|
|
ENST00000343257.7:c.2914G>C
MANE Select
|
ENSP00000339867.2:p.Gly972Arg
|
|
ENST00000343257.6:c.2914G>C
|
ENSP00000339867.2:p.Gly972Arg
|
|
NM_000083.2:c.2914G>C
|
NP_000074.2:p.Gly972Arg
|
|
NR_046453.1:n.2854G>C
|
|
|
XM_011515781.1:c.2938G>C
|
XP_011514083.1:p.Gly980Arg
|
|
XM_011515782.1:c.1660G>C
|
XP_011514084.1:p.Gly554Arg
|
|
XM_011515782.2:c.1660G>C
|
XP_011514084.1:p.Gly554Arg
|
|
XM_017011739.1:c.2488G>C
|
XP_016867228.1:p.Gly830Arg
|
|
XM_017011740.1:c.2464G>C
|
XP_016867229.1:p.Gly822Arg
|
|
NM_000083.3:c.2914G>C
MANE Select
|
NP_000074.3:p.Gly972Arg
|
|
NR_046453.2:n.2869G>C
|
|
|