ENST00000703783.1:n.909T>C
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|
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ENST00000703785.1:n.990T>C
|
|
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ENST00000262464.9:c.4125T>C
MANE Select
|
ENSP00000262464.4:p.Ala1375=
|
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ENST00000262464.8:c.4125T>C
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ENSP00000262464.4:p.Ala1375=
|
|
ENST00000507835.5:c.675T>C
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ENSP00000426839.1:p.Ala225=
|
|
ENST00000508053.5:c.4125T>C
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ENSP00000424571.1:p.Ala1375=
|
|
ENST00000508989.5:c.4026T>C
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ENSP00000425596.1:p.Ala1342=
|
|
ENST00000619499.4:c.4122T>C
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ENSP00000482132.1:p.Ala1374=
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|
NM_001999.3:c.4125T>C
|
NP_001990.2:p.Ala1375=
|
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XM_017009228.2:c.3972T>C
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XP_016864717.1:p.Ala1324=
|
|
NM_001999.4:c.4125T>C
MANE Select
|
NP_001990.2:p.Ala1375=
|
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