ENST00000265171.10:c.*149G>C
MANE Select
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ENSP00000265171.5:n.*149G>C
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|
ENST00000652245.1:c.*292G>C
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ENSP00000498337.1:n.*292G>C
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|
ENST00000265171.9:c.*149G>C
|
ENSP00000265171.5:n.*149G>C
|
|
ENST00000509793.5:c.*149G>C
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ENSP00000424316.1:n.*149G>C
|
|
ENST00000509996.1:n.1379G>C
|
|
|
ENST00000540840.1:n.229+296G>C
|
|
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NM_001178130.1:c.*149G>C
|
NP_001171601.1:n.*149G>C
|
|
NM_001178131.1:c.*149G>C
|
NP_001171602.1:n.*149G>C
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|
NM_001963.4:c.*149G>C
|
NP_001954.2:n.*149G>C
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|
XM_005262796.2:c.*149G>C
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XP_005262853.1:n.*149G>C
|
|
XM_005262797.2:c.*149G>C
|
XP_005262854.1:n.*149G>C
|
|
XM_005262798.2:c.*149G>C
|
XP_005262855.1:n.*149G>C
|
|
XM_005262800.2:c.*292G>C
|
XP_005262857.1:n.*292G>C
|
|
XM_005262801.2:c.*149G>C
|
XP_005262858.1:n.*149G>C
|
|
XM_006714124.2:c.*292G>C
|
XP_006714187.1:n.*292G>C
|
|
XM_011531707.1:c.*149G>C
|
XP_011530009.1:n.*149G>C
|
|
NM_001178130.2:c.*149G>C
|
NP_001171601.1:n.*149G>C
|
|
NM_001178131.2:c.*149G>C
|
NP_001171602.1:n.*149G>C
|
|
NM_001357021.1:c.*292G>C
|
NP_001343950.1:n.*292G>C
|
|
NM_001963.5:c.*149G>C
|
NP_001954.2:n.*149G>C
|
|
XM_017007845.1:c.*149G>C
|
XP_016863334.1:n.*149G>C
|
|
XM_017007846.1:c.*149G>C
|
XP_016863335.1:n.*149G>C
|
|
XM_017007847.1:c.*149G>C
|
XP_016863336.1:n.*149G>C
|
|
XM_017007848.1:c.*149G>C
|
XP_016863337.1:n.*149G>C
|
|
XM_017007849.1:c.*149G>C
|
XP_016863338.1:n.*149G>C
|
|
XM_017007850.1:c.*292G>C
|
XP_016863339.1:n.*292G>C
|
|
XM_017007851.1:c.*292G>C
|
XP_016863340.1:n.*292G>C
|
|
NM_001178130.3:c.*149G>C
|
NP_001171601.1:n.*149G>C
|
|
NM_001178131.3:c.*149G>C
|
NP_001171602.1:n.*149G>C
|
|
NM_001357021.2:c.*292G>C
|
NP_001343950.1:n.*292G>C
|
|
NM_001963.6:c.*149G>C
MANE Select
|
NP_001954.2:n.*149G>C
|
|