ENST00000650516.2:c.1643A>C
|
ENSP00000498052.2:p.Glu548Ala
|
|
ENST00000343257.7:c.1643A>C
MANE Select
|
ENSP00000339867.2:p.Glu548Ala
|
|
ENST00000432192.6:c.1467A>C
|
|
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ENST00000343257.6:c.1643A>C
|
ENSP00000339867.2:p.Glu548Ala
|
|
NM_000083.2:c.1643A>C
|
NP_000074.2:p.Glu548Ala
|
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NR_046453.1:n.1583A>C
|
|
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XM_011515781.1:c.1667A>C
|
XP_011514083.1:p.Glu556Ala
|
|
XM_011515782.1:c.389A>C
|
XP_011514084.1:p.Glu130Ala
|
|
XM_011515782.2:c.389A>C
|
XP_011514084.1:p.Glu130Ala
|
|
XM_017011739.1:c.1217A>C
|
XP_016867228.1:p.Glu406Ala
|
|
XM_017011740.1:c.1193A>C
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XP_016867229.1:p.Glu398Ala
|
|
NM_000083.3:c.1643A>C
MANE Select
|
NP_000074.3:p.Glu548Ala
|
|
NR_046453.2:n.1598A>C
|
|
|