ENST00000318158.11:c.528T>A
MANE Select
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ENSP00000313432.6:p.Gly176=
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ENST00000318158.10:c.528T>A
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ENSP00000313432.6:p.Gly176=
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|
ENST00000377824.8:n.565T>A
|
|
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ENST00000460882.5:n.555T>A
|
|
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ENST00000480596.5:n.1229T>A
|
|
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ENST00000491488.5:n.233T>A
|
|
|
ENST00000494290.1:c.99T>A
|
ENSP00000432021.1:p.Gly33=
|
|
ENST00000497693.1:n.2061T>A
|
|
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ENST00000607784.1:c.528T>A
|
ENSP00000475569.1:p.Gly176=
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|
NM_012203.1:c.528T>A
|
NP_036335.1:p.Gly176=
|
|
XM_005251631.1:c.207T>A
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XP_005251688.1:p.Gly69=
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XM_011518073.1:c.126T>A
|
XP_011516375.1:p.Gly42=
|
|
XR_929374.1:n.973T>A
|
|
|
XM_017015320.2:c.528T>A
|
XP_016870809.1:p.Gly176=
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|
XM_017015321.2:c.528T>A
|
XP_016870810.1:p.Gly176=
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|
XM_017015323.2:c.126T>A
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XP_016870812.1:p.Gly42=
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|
XM_024447716.1:c.801T>A
|
XP_024303484.1:p.Gly267=
|
|
XM_024447717.1:c.801T>A
|
XP_024303485.1:p.Gly267=
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|
XR_002956828.1:n.816T>A
|
|
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XR_002956829.1:n.816T>A
|
|
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XR_002956830.1:n.587T>A
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XR_002956831.1:n.262T>A
|
|
|
XR_002956832.1:n.947T>A
|
|
|
NM_012203.2:c.528T>A
MANE Select
|
NP_036335.1:p.Gly176=
|
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