ENST00000316386.11:c.*964T>C
MANE Select
|
ENSP00000319476.6:n.*964T>C
|
|
ENST00000316386.10:c.*964T>C
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ENSP00000319476.6:n.*964T>C
|
|
ENST00000435193.1:c.*972T>C
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ENSP00000415951.1:n.*972T>C
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|
NM_012092.3:c.*964T>C , LRG_65t1:c.*964T>C
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NP_036224.1:n.*964T>C
|
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XM_011511028.1:c.*1065T>C
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XP_011509330.1:n.*1065T>C
|
|
XM_011511029.1:c.*964T>C
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XP_011509331.1:n.*964T>C
|
|
XM_011511030.1:c.*1065T>C
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XP_011509332.1:n.*1065T>C
|
|
XM_011511031.1:c.*1065T>C
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XP_011509333.1:n.*1065T>C
|
|
NM_012092.4:c.*964T>C
MANE Select
|
NP_036224.1:n.*964T>C
|
|