ENST00000645828.1:n.2772T>G
|
|
|
ENST00000651671.1:c.4965T>G
MANE Select
|
ENSP00000498587.1:p.Gly1655=
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|
ENST00000679595.1:c.4965T>G
|
ENSP00000506241.1:p.Gly1655=
|
|
ENST00000680133.1:c.4851T>G
|
ENSP00000505319.1:p.Gly1617=
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|
ENST00000680218.1:c.4845T>G
|
ENSP00000505339.1:p.Gly1615=
|
|
ENST00000680668.1:c.4851T>G
|
ENSP00000506336.1:p.Gly1617=
|
|
ENST00000680778.1:c.2562T>G
|
ENSP00000506033.1:p.Gly854=
|
|
ENST00000680924.1:c.*2365T>G
|
ENSP00000506031.1:n.*2365T>G
|
|
ENST00000681135.1:c.*2574T>G
|
ENSP00000506636.1:n.*2574T>G
|
|
ENST00000681298.1:n.1778T>G
|
|
|
ENST00000681454.1:c.*4201T>G
|
ENSP00000505763.1:n.*4201T>G
|
|
ENST00000277541.6:c.4965T>G
|
ENSP00000277541.6:p.Gly1655=
|
|
ENST00000494783.1:n.120T>G
|
|
|
NM_017617.3:c.4965T>G
|
NP_060087.3:p.Gly1655=
|
|
XM_011518717.1:c.4266T>G
|
XP_011517019.1:p.Gly1422=
|
|
NM_017617.5:c.4965T>G
MANE Select
|
NP_060087.3:p.Gly1655=
|
|
XM_011518717.2:c.4242T>G
|
XP_011517019.2:p.Gly1414=
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