ENST00000650516.2:c.2913G>C
|
ENSP00000498052.2:p.Gln971His
|
|
ENST00000343257.7:c.2913G>C
MANE Select
|
ENSP00000339867.2:p.Gln971His
|
|
ENST00000343257.6:c.2913G>C
|
ENSP00000339867.2:p.Gln971His
|
|
NM_000083.2:c.2913G>C
|
NP_000074.2:p.Gln971His
|
|
NR_046453.1:n.2853G>C
|
|
|
XM_011515781.1:c.2937G>C
|
XP_011514083.1:p.Gln979His
|
|
XM_011515782.1:c.1659G>C
|
XP_011514084.1:p.Gln553His
|
|
XM_011515782.2:c.1659G>C
|
XP_011514084.1:p.Gln553His
|
|
XM_017011739.1:c.2487G>C
|
XP_016867228.1:p.Gln829His
|
|
XM_017011740.1:c.2463G>C
|
XP_016867229.1:p.Gln821His
|
|
NM_000083.3:c.2913G>C
MANE Select
|
NP_000074.3:p.Gln971His
|
|
NR_046453.2:n.2868G>C
|
|
|