ENST00000650516.2:c.2696C>G
|
ENSP00000498052.2:p.Ala899Gly
|
|
ENST00000343257.7:c.2696C>G
MANE Select
|
ENSP00000339867.2:p.Ala899Gly
|
|
ENST00000432192.6:c.2520C>G
|
|
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ENST00000343257.6:c.2696C>G
|
ENSP00000339867.2:p.Ala899Gly
|
|
NM_000083.2:c.2696C>G
|
NP_000074.2:p.Ala899Gly
|
|
NR_046453.1:n.2636C>G
|
|
|
XM_011515781.1:c.2720C>G
|
XP_011514083.1:p.Ala907Gly
|
|
XM_011515782.1:c.1442C>G
|
XP_011514084.1:p.Ala481Gly
|
|
XM_011515782.2:c.1442C>G
|
XP_011514084.1:p.Ala481Gly
|
|
XM_017011739.1:c.2270C>G
|
XP_016867228.1:p.Ala757Gly
|
|
XM_017011740.1:c.2246C>G
|
XP_016867229.1:p.Ala749Gly
|
|
NM_000083.3:c.2696C>G
MANE Select
|
NP_000074.3:p.Ala899Gly
|
|
NR_046453.2:n.2651C>G
|
|
|