ENST00000318158.11:c.513T>C
MANE Select
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ENSP00000313432.6:p.Arg171=
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ENST00000318158.10:c.513T>C
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ENSP00000313432.6:p.Arg171=
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ENST00000377824.8:n.550T>C
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ENST00000460882.5:n.540T>C
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ENST00000480596.5:n.1214T>C
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|
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ENST00000491488.5:n.218T>C
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ENST00000494290.1:c.84T>C
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ENSP00000432021.1:p.Arg28=
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ENST00000497693.1:n.2046T>C
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|
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ENST00000607784.1:c.513T>C
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ENSP00000475569.1:p.Arg171=
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NM_012203.1:c.513T>C
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NP_036335.1:p.Arg171=
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XM_005251631.1:c.192T>C
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XP_005251688.1:p.Arg64=
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XM_011518073.1:c.111T>C
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XP_011516375.1:p.Arg37=
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XR_929374.1:n.958T>C
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|
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XM_017015320.2:c.513T>C
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XP_016870809.1:p.Arg171=
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XM_017015321.2:c.513T>C
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XP_016870810.1:p.Arg171=
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XM_017015323.2:c.111T>C
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XP_016870812.1:p.Arg37=
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XM_024447716.1:c.786T>C
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XP_024303484.1:p.Arg262=
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XM_024447717.1:c.786T>C
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XP_024303485.1:p.Arg262=
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XR_002956828.1:n.801T>C
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XR_002956829.1:n.801T>C
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XR_002956830.1:n.572T>C
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XR_002956831.1:n.247T>C
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XR_002956832.1:n.932T>C
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NM_012203.2:c.513T>C
MANE Select
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NP_036335.1:p.Arg171=
|
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