ENST00000318158.11:c.495C>T
MANE Select
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ENSP00000313432.6:p.Gly165=
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|
ENST00000318158.10:c.495C>T
|
ENSP00000313432.6:p.Gly165=
|
|
ENST00000377824.8:n.532C>T
|
|
|
ENST00000460882.5:n.522C>T
|
|
|
ENST00000480596.5:n.1196C>T
|
|
|
ENST00000491488.5:n.200C>T
|
|
|
ENST00000494290.1:c.66C>T
|
ENSP00000432021.1:p.Gly22=
|
|
ENST00000497693.1:n.2028C>T
|
|
|
ENST00000607784.1:c.495C>T
|
ENSP00000475569.1:p.Gly165=
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|
NM_012203.1:c.495C>T
|
NP_036335.1:p.Gly165=
|
|
XM_005251631.1:c.174C>T
|
XP_005251688.1:p.Gly58=
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|
XM_011518073.1:c.93C>T
|
XP_011516375.1:p.Gly31=
|
|
XR_929374.1:n.940C>T
|
|
|
XM_017015320.2:c.495C>T
|
XP_016870809.1:p.Gly165=
|
|
XM_017015321.2:c.495C>T
|
XP_016870810.1:p.Gly165=
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|
XM_017015323.2:c.93C>T
|
XP_016870812.1:p.Gly31=
|
|
XM_024447716.1:c.768C>T
|
XP_024303484.1:p.Gly256=
|
|
XM_024447717.1:c.768C>T
|
XP_024303485.1:p.Gly256=
|
|
XR_002956828.1:n.783C>T
|
|
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XR_002956829.1:n.783C>T
|
|
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XR_002956830.1:n.554C>T
|
|
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XR_002956831.1:n.229C>T
|
|
|
XR_002956832.1:n.914C>T
|
|
|
NM_012203.2:c.495C>T
MANE Select
|
NP_036335.1:p.Gly165=
|
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