ENST00000318158.11:c.444C>G
MANE Select
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ENSP00000313432.6:p.Gly148=
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ENST00000318158.10:c.444C>G
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ENSP00000313432.6:p.Gly148=
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ENST00000377824.8:n.481C>G
|
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ENST00000460882.5:n.471C>G
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|
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ENST00000491488.5:n.149C>G
|
|
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ENST00000493368.5:n.501C>G
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ENST00000497693.1:n.818C>G
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|
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ENST00000607784.1:c.444C>G
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ENSP00000475569.1:p.Gly148=
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NM_012203.1:c.444C>G
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NP_036335.1:p.Gly148=
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XM_005251631.1:c.123C>G
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XP_005251688.1:p.Gly41=
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XM_011518073.1:c.-319C>G
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XP_011516375.1:n.-319C>G
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XR_929374.1:n.529C>G
|
|
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XM_017015320.2:c.444C>G
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XP_016870809.1:p.Gly148=
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XM_017015321.2:c.444C>G
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XP_016870810.1:p.Gly148=
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XM_017015323.2:c.-319C>G
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XP_016870812.1:n.-319C>G
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XM_024447716.1:c.717C>G
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XP_024303484.1:p.Gly239=
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XM_024447717.1:c.717C>G
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XP_024303485.1:p.Gly239=
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XR_002956828.1:n.732C>G
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XR_002956829.1:n.732C>G
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XR_002956830.1:n.503C>G
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XR_002956831.1:n.178C>G
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XR_002956832.1:n.503C>G
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NM_012203.2:c.444C>G
MANE Select
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NP_036335.1:p.Gly148=
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