ENST00000493477.2:n.636G=
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|
|
ENST00000682162.1:c.162G=
|
ENSP00000508203.1:p.Arg54=
|
|
ENST00000682567.1:n.210G=
|
|
|
ENST00000683521.1:c.133G=
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ENSP00000506864.1:p.Ala45=
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|
ENST00000684483.1:c.133G=
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ENSP00000507894.1:p.Ala45=
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|
ENST00000366560.4:c.133G=
MANE Select
|
ENSP00000355518.4:p.Ala45=
|
|
ENST00000366560.3:c.133G=
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ENSP00000355518.3:p.Ala45=
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|
ENST00000493477.1:n.246G=
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|
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NM_000143.3:c.133G= , LRG_504t1:c.133G=
|
NP_000134.2:p.Ala45=
|
|
XM_011544132.1:c.-96G=
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XP_011542434.1:n.-96G=
|
|
XM_011544132.2:c.-96G=
|
XP_011542434.1:n.-96G=
|
|
NM_000143.4:c.133G=
MANE Select
|
NP_000134.2:p.Ala45=
|
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