ENST00000645828.1:n.2773G>T
|
|
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ENST00000651671.1:c.4966G>T
MANE Select
|
ENSP00000498587.1:p.Gly1656Cys
|
|
ENST00000679595.1:c.4966G>T
|
ENSP00000506241.1:p.Gly1656Cys
|
|
ENST00000680133.1:c.4852G>T
|
ENSP00000505319.1:p.Gly1618Cys
|
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ENST00000680218.1:c.4846G>T
|
ENSP00000505339.1:p.Gly1616Cys
|
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ENST00000680668.1:c.4852G>T
|
ENSP00000506336.1:p.Gly1618Cys
|
|
ENST00000680778.1:c.2563G>T
|
ENSP00000506033.1:p.Gly855Cys
|
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ENST00000680924.1:c.*2366G>T
|
ENSP00000506031.1:n.*2366G>T
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ENST00000681135.1:c.*2575G>T
|
ENSP00000506636.1:n.*2575G>T
|
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ENST00000681298.1:n.1779G>T
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|
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ENST00000681454.1:c.*4202G>T
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ENSP00000505763.1:n.*4202G>T
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ENST00000277541.6:c.4966G>T
|
ENSP00000277541.6:p.Gly1656Cys
|
|
ENST00000494783.1:n.121G>T
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|
|
NM_017617.3:c.4966G>T
|
NP_060087.3:p.Gly1656Cys
|
|
XM_011518717.1:c.4267G>T
|
XP_011517019.1:p.Gly1423Cys
|
|
NM_017617.5:c.4966G>T
MANE Select
|
NP_060087.3:p.Gly1656Cys
|
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XM_011518717.2:c.4243G>T
|
XP_011517019.2:p.Gly1415Cys
|
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