ENST00000260950.5:c.712G>A
(MSTN)
MANE Select
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ENSP00000260950.3:p.Ala238Thr
|
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ENST00000260950.4:c.712G>A
(MSTN)
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ENSP00000260950.3:p.Ala238Thr
|
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ENST00000478197.1:n.220-19126C>T
(C2orf88)
|
|
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ENST00000495546.1:n.202-19857C>T
(C2orf88)
|
|
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NM_005259.2:c.712G>A , LRG_200t1:c.712G>A
(MSTN)
|
NP_005250.1:p.Ala238Thr
|
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XM_005246905.1:c.-359-19857C>T
(C2orf88)
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XP_005246962.1:n.-359-19857C>T
|
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XM_011510958.1:c.328G>A
(MSTN)
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XP_011509260.1:p.Ala110Thr
|
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XM_011511982.1:c.-433-19857C>T
(C2orf88)
|
XP_011510284.1:n.-433-19857C>T
|
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XM_011511986.1:c.-234-19857C>T
(C2orf88)
|
XP_011510288.1:n.-234-19857C>T
|
|
XM_011511986.2:c.-234-19857C>T
(C2orf88)
|
XP_011510288.1:n.-234-19857C>T
|
|
NM_005259.3:c.712G>A
(MSTN)
MANE Select
|
NP_005250.1:p.Ala238Thr
|
|