ENST00000318158.11:c.*184T>C
MANE Select
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ENSP00000313432.6:n.*184T>C
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ENST00000318158.10:c.*184T>C
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ENSP00000313432.6:n.*184T>C
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|
ENST00000480596.5:n.1872T>C
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|
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ENST00000494290.1:c.*137T>C
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ENSP00000432021.1:n.*137T>C
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ENST00000497693.1:n.4739T>C
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|
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NM_012203.1:c.*184T>C
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NP_036335.1:n.*184T>C
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XM_005251631.1:c.*184T>C
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XP_005251688.1:n.*184T>C
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XM_011518073.1:c.*184T>C
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XP_011516375.1:n.*184T>C
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XM_017015320.2:c.946-445T>C
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XP_016870809.1:n.946-445T>C
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XM_017015321.2:c.866-445T>C
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XP_016870810.1:n.866-445T>C
|
|
XM_017015323.2:c.544-445T>C
|
XP_016870812.1:n.544-445T>C
|
|
XM_024447716.1:c.1219-445T>C
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XP_024303484.1:n.1219-445T>C
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XM_024447717.1:c.1139-445T>C
|
XP_024303485.1:n.1139-445T>C
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XR_002956828.1:n.1234-445T>C
|
|
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XR_002956829.1:n.1154-445T>C
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XR_002956830.1:n.2591T>C
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|
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XR_002956831.1:n.2266T>C
|
|
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XR_002956832.1:n.1590T>C
|
|
|
NM_012203.2:c.*184T>C
MANE Select
|
NP_036335.1:n.*184T>C
|
|