ENST00000646743.1:c.184G>A
MANE Select
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ENSP00000495564.1:p.Ala62Thr
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ENST00000251808.7:c.184G>A
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ENSP00000251808.3:p.Ala62Thr
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ENST00000395927.1:c.136G>A
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ENSP00000379260.1:p.Ala46Thr
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ENST00000472106.2:n.512G>A
|
|
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NM_024915.3:c.184G>A
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NP_079191.2:p.Ala62Thr
|
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XM_011517305.1:c.136G>A
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XP_011515607.1:p.Ala46Thr
|
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XM_011517306.1:c.136G>A
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XP_011515608.1:p.Ala46Thr
|
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XM_011517307.1:c.184G>A
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XP_011515609.1:p.Ala62Thr
|
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NM_001330593.1:c.136G>A
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NP_001317522.1:p.Ala46Thr
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XM_011517306.3:c.136G>A
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XP_011515608.1:p.Ala46Thr
|
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XM_011517307.3:c.184G>A
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XP_011515609.1:p.Ala62Thr
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NM_001330593.2:c.136G>A
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NP_001317522.1:p.Ala46Thr
|
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NM_024915.4:c.184G>A
MANE Select
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NP_079191.2:p.Ala62Thr
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