ENST00000703783.1:n.629C>T
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|
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ENST00000703785.1:n.710C>T
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|
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ENST00000262464.9:c.3845C>T
MANE Select
|
ENSP00000262464.4:p.Ala1282Val
|
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ENST00000262464.8:c.3845C>T
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ENSP00000262464.4:p.Ala1282Val
|
|
ENST00000507835.5:c.395C>T
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ENSP00000426839.1:p.Ala132Val
|
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ENST00000508053.5:c.3845C>T
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ENSP00000424571.1:p.Ala1282Val
|
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ENST00000508989.5:c.3746C>T
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ENSP00000425596.1:p.Ala1249Val
|
|
ENST00000619499.4:c.3842C>T
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ENSP00000482132.1:p.Ala1281Val
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NM_001999.3:c.3845C>T
|
NP_001990.2:p.Ala1282Val
|
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XM_017009228.2:c.3692C>T
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XP_016864717.1:p.Ala1231Val
|
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NM_001999.4:c.3845C>T
MANE Select
|
NP_001990.2:p.Ala1282Val
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