ENST00000598239.6:c.*316G>C
MANE Select
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ENSP00000469315.1:n.*316G>C
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|
ENST00000695963.1:n.815G>C
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|
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ENST00000695964.1:n.678G>C
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|
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ENST00000695965.1:c.*316G>C
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ENSP00000512291.1:n.*316G>C
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ENST00000695998.1:c.*316G>C
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ENSP00000512319.1:n.*316G>C
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ENST00000326856.8:c.*316G>C
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ENSP00000314783.4:n.*316G>C
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ENST00000601680.1:n.1207G>C
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NM_001277081.1:c.*316G>C
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NP_001264010.1:n.*316G>C
|
|
NM_001277082.1:c.*464G>C
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NP_001264011.1:n.*464G>C
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|
NM_017509.3:c.*316G>C
|
NP_059979.2:n.*316G>C
|
|
NR_102274.1:n.997G>C
|
|
|
XM_006723265.2:c.*316G>C
|
XP_006723328.1:n.*316G>C
|
|
XM_011527083.1:c.*316G>C
|
XP_011525385.1:n.*316G>C
|
|
XM_011527084.1:c.*316G>C
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XP_011525386.1:n.*316G>C
|
|
XM_011527085.1:c.*316G>C
|
XP_011525387.1:n.*316G>C
|
|
XM_011527086.1:c.*316G>C
|
XP_011525388.1:n.*316G>C
|
|
XM_011527087.1:c.*316G>C
|
XP_011525389.1:n.*316G>C
|
|
XM_011527089.1:c.*464G>C
|
XP_011525391.1:n.*464G>C
|
|
XM_011527090.1:c.*316G>C
|
XP_011525392.1:n.*316G>C
|
|
XM_006723265.3:c.*316G>C
|
XP_006723328.1:n.*316G>C
|
|
XM_011527085.2:c.*316G>C
|
XP_011525387.1:n.*316G>C
|
|
XM_011527087.2:c.*316G>C
|
XP_011525389.1:n.*316G>C
|
|
XM_011527089.2:c.*464G>C
|
XP_011525391.1:n.*464G>C
|
|
XR_001753713.1:n.1808G>C
|
|
|
NM_001277081.2:c.*316G>C
|
NP_001264010.1:n.*316G>C
|
|
NM_001277082.2:c.*464G>C
|
NP_001264011.1:n.*464G>C
|
|
NM_017509.4:c.*316G>C
MANE Select
|
NP_059979.2:n.*316G>C
|
|