ENST00000309539.8:c.*171A>C
MANE Select
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ENSP00000309124.3:n.*171A>C
|
|
ENST00000309539.7:c.*171A>C
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ENSP00000309124.3:n.*171A>C
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|
ENST00000432556.6:c.*307A>C
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ENSP00000405116.2:n.*307A>C
|
|
ENST00000536989.1:n.528A>C
|
|
|
ENST00000543993.5:c.*307A>C
|
ENSP00000445085.1:n.*307A>C
|
|
ENST00000544577.5:c.*171A>C
|
ENSP00000444457.1:n.*171A>C
|
|
ENST00000545927.5:c.*307A>C
|
ENSP00000439251.1:n.*307A>C
|
|
NM_001172632.1:c.*307A>C
|
NP_001166103.1:n.*307A>C
|
|
NM_001172633.1:c.*307A>C
|
NP_001166104.1:n.*307A>C
|
|
NM_002543.3:c.*171A>C
|
NP_002534.1:n.*171A>C
|
|
XM_011520682.1:c.*171A>C
|
XP_011518984.1:n.*171A>C
|
|
XM_011520683.1:c.*323A>C
|
XP_011518985.1:n.*323A>C
|
|
NM_002543.4:c.*171A>C
MANE Select
|
NP_002534.1:n.*171A>C
|
|
NM_001172632.2:c.*307A>C
|
NP_001166103.1:n.*307A>C
|
|
NM_001172633.2:c.*307A>C
|
NP_001166104.1:n.*307A>C
|
|