ENST00000561514.3:c.*20A>C
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ENSP00000460666.3:n.*20A>C
|
|
ENST00000565038.2:c.*1066A>C
|
ENSP00000459882.2:n.*1066A>C
|
|
ENST00000566069.6:c.*216A>C
|
ENSP00000459237.2:n.*216A>C
|
|
ENST00000697377.2:c.*20A>C
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ENSP00000513286.2:n.*20A>C
|
|
ENST00000697379.2:c.*20A>C
|
ENSP00000513287.2:n.*20A>C
|
|
ENST00000561514.2:c.*20A>C
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ENSP00000460666.2:n.*20A>C
|
|
ENST00000697374.1:c.*20A>C
|
ENSP00000513284.1:n.*20A>C
|
|
ENST00000697375.1:n.4928A>C
|
|
|
ENST00000697376.1:c.*216A>C
|
ENSP00000513285.1:n.*216A>C
|
|
ENST00000697377.1:c.*20A>C
|
ENSP00000513286.1:n.*20A>C
|
|
ENST00000697378.1:n.4101A>C
|
|
|
ENST00000697379.1:c.*20A>C
|
ENSP00000513287.1:n.*20A>C
|
|
ENST00000697380.1:n.2785A>C
|
|
|
ENST00000697381.1:n.2276A>C
|
|
|
ENST00000697382.1:c.*358A>C
|
ENSP00000513288.1:n.*358A>C
|
|
ENST00000697383.1:c.*20A>C
|
ENSP00000513289.1:n.*20A>C
|
|
ENST00000261584.9:c.*20A>C
MANE Select
|
ENSP00000261584.4:n.*20A>C
|
|
ENST00000261584.8:c.*20A>C
|
ENSP00000261584.4:n.*20A>C
|
|
ENST00000566069.5:c.347A>C
|
|
|
ENST00000568219.5:c.*20A>C
|
ENSP00000454703.2:n.*20A>C
|
|
NM_024675.3:c.*20A>C , LRG_308t1:c.*20A>C
|
NP_078951.2:n.*20A>C
|
|
XM_011545946.1:c.*20A>C
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XP_011544248.1:n.*20A>C
|
|
XM_011545947.1:c.*216A>C
|
XP_011544249.1:n.*216A>C
|
|
XM_011545948.1:c.*20A>C
|
XP_011544250.1:n.*20A>C
|
|
XR_950851.1:n.4289A>C
|
|
|
XM_011545946.2:c.*20A>C
|
XP_011544248.1:n.*20A>C
|
|
XM_011545947.2:c.*216A>C
|
XP_011544249.1:n.*216A>C
|
|
XM_011545948.2:c.*20A>C
|
XP_011544250.1:n.*20A>C
|
|
XM_017023671.1:c.*20A>C
|
XP_016879160.1:n.*20A>C
|
|
XM_017023672.2:c.*20A>C
|
XP_016879161.1:n.*20A>C
|
|
XM_017023673.2:c.*216A>C
|
XP_016879162.1:n.*216A>C
|
|
NM_024675.4:c.*20A>C
MANE Select
|
NP_078951.2:n.*20A>C
|
|