ENST00000650516.2:c.2939A>G
|
ENSP00000498052.2:p.Glu980Gly
|
|
ENST00000343257.7:c.2939A>G
MANE Select
|
ENSP00000339867.2:p.Glu980Gly
|
|
ENST00000343257.6:c.2939A>G
|
ENSP00000339867.2:p.Glu980Gly
|
|
NM_000083.2:c.2939A>G
|
NP_000074.2:p.Glu980Gly
|
|
NR_046453.1:n.2879A>G
|
|
|
XM_011515781.1:c.2963A>G
|
XP_011514083.1:p.Glu988Gly
|
|
XM_011515782.1:c.1685A>G
|
XP_011514084.1:p.Glu562Gly
|
|
XM_011515782.2:c.1685A>G
|
XP_011514084.1:p.Glu562Gly
|
|
XM_017011739.1:c.2513A>G
|
XP_016867228.1:p.Glu838Gly
|
|
XM_017011740.1:c.2489A>G
|
XP_016867229.1:p.Glu830Gly
|
|
NM_000083.3:c.2939A>G
MANE Select
|
NP_000074.3:p.Glu980Gly
|
|
NR_046453.2:n.2894A>G
|
|
|