ENST00000493477.2:n.1001A>G
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|
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ENST00000682162.1:c.527A>G
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ENSP00000508203.1:n.527A>G
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ENST00000682567.1:n.575A>G
|
|
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ENST00000683521.1:c.498A>G
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ENSP00000506864.1:p.Gly166=
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ENST00000684483.1:c.498A>G
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ENSP00000507894.1:p.Gly166=
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ENST00000366560.4:c.498A>G
MANE Select
|
ENSP00000355518.4:p.Gly166=
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|
ENST00000366560.3:c.498A>G
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ENSP00000355518.3:p.Gly166=
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ENST00000497042.1:n.194A>G
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|
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NM_000143.3:c.498A>G , LRG_504t1:c.498A>G
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NP_000134.2:p.Gly166=
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|
XM_011544132.1:c.270A>G
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XP_011542434.1:p.Gly90=
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|
XM_011544132.2:c.270A>G
|
XP_011542434.1:p.Gly90=
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|
NM_000143.4:c.498A>G
MANE Select
|
NP_000134.2:p.Gly166=
|
|