ENST00000318158.11:c.469G>T
MANE Select
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ENSP00000313432.6:p.Gly157Cys
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ENST00000318158.10:c.469G>T
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ENSP00000313432.6:p.Gly157Cys
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ENST00000377824.8:n.506G>T
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ENST00000460882.5:n.496G>T
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ENST00000480596.5:n.11G>T
|
|
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ENST00000491488.5:n.174G>T
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ENST00000493368.5:n.526G>T
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ENST00000497693.1:n.843G>T
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ENST00000607784.1:c.469G>T
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ENSP00000475569.1:p.Gly157Cys
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NM_012203.1:c.469G>T
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NP_036335.1:p.Gly157Cys
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XM_005251631.1:c.148G>T
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XP_005251688.1:p.Gly50Cys
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XM_011518073.1:c.-294G>T
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XP_011516375.1:n.-294G>T
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XR_929374.1:n.554G>T
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XM_017015320.2:c.469G>T
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XP_016870809.1:p.Gly157Cys
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XM_017015321.2:c.469G>T
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XP_016870810.1:p.Gly157Cys
|
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XM_017015323.2:c.-294G>T
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XP_016870812.1:n.-294G>T
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XM_024447716.1:c.742G>T
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XP_024303484.1:p.Gly248Cys
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XM_024447717.1:c.742G>T
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XP_024303485.1:p.Gly248Cys
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XR_002956828.1:n.757G>T
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XR_002956829.1:n.757G>T
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XR_002956830.1:n.528G>T
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XR_002956831.1:n.203G>T
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XR_002956832.1:n.528G>T
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NM_012203.2:c.469G>T
MANE Select
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NP_036335.1:p.Gly157Cys
|
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