ENST00000650516.2:c.1627G=
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ENSP00000498052.2:p.Ala543=
|
|
ENST00000343257.7:c.1627G=
MANE Select
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ENSP00000339867.2:p.Ala543=
|
|
ENST00000432192.6:c.1451G=
|
|
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ENST00000343257.6:c.1627G=
|
ENSP00000339867.2:p.Ala543=
|
|
NM_000083.2:c.1627G=
|
NP_000074.2:p.Ala543=
|
|
NR_046453.1:n.1567G=
|
|
|
XM_011515781.1:c.1651G=
|
XP_011514083.1:p.Ala551=
|
|
XM_011515782.1:c.373G=
|
XP_011514084.1:p.Ala125=
|
|
XM_011515782.2:c.373G=
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XP_011514084.1:p.Ala125=
|
|
XM_017011739.1:c.1201G=
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XP_016867228.1:p.Ala401=
|
|
XM_017011740.1:c.1177G=
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XP_016867229.1:p.Ala393=
|
|
NM_000083.3:c.1627G=
MANE Select
|
NP_000074.3:p.Ala543=
|
|
NR_046453.2:n.1582G=
|
|
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