ENST00000650516.2:c.2534G>C
|
ENSP00000498052.2:p.Gly845Ala
|
|
ENST00000343257.7:c.2534G>C
MANE Select
|
ENSP00000339867.2:p.Gly845Ala
|
|
ENST00000432192.6:c.2358G>C
|
|
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ENST00000343257.6:c.2534G>C
|
ENSP00000339867.2:p.Gly845Ala
|
|
NM_000083.2:c.2534G>C
|
NP_000074.2:p.Gly845Ala
|
|
NR_046453.1:n.2474G>C
|
|
|
XM_011515781.1:c.2558G>C
|
XP_011514083.1:p.Gly853Ala
|
|
XM_011515782.1:c.1280G>C
|
XP_011514084.1:p.Gly427Ala
|
|
XM_011515782.2:c.1280G>C
|
XP_011514084.1:p.Gly427Ala
|
|
XM_017011739.1:c.2108G>C
|
XP_016867228.1:p.Gly703Ala
|
|
XM_017011740.1:c.2084G>C
|
XP_016867229.1:p.Gly695Ala
|
|
NM_000083.3:c.2534G>C
MANE Select
|
NP_000074.3:p.Gly845Ala
|
|
NR_046453.2:n.2489G>C
|
|
|