ENST00000650516.2:c.2785A>G
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ENSP00000498052.2:p.Thr929Ala
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ENST00000343257.7:c.2785A>G
MANE Select
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ENSP00000339867.2:p.Thr929Ala
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ENST00000343257.6:c.2785A>G
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ENSP00000339867.2:p.Thr929Ala
|
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NM_000083.2:c.2785A>G
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NP_000074.2:p.Thr929Ala
|
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NR_046453.1:n.2725A>G
|
|
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XM_011515781.1:c.2809A>G
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XP_011514083.1:p.Thr937Ala
|
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XM_011515782.1:c.1531A>G
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XP_011514084.1:p.Thr511Ala
|
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XM_011515782.2:c.1531A>G
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XP_011514084.1:p.Thr511Ala
|
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XM_017011739.1:c.2359A>G
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XP_016867228.1:p.Thr787Ala
|
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XM_017011740.1:c.2335A>G
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XP_016867229.1:p.Thr779Ala
|
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NM_000083.3:c.2785A>G
MANE Select
|
NP_000074.3:p.Thr929Ala
|
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NR_046453.2:n.2740A>G
|
|
|