ENST00000311066.10:c.*1362T>G
MANE Select
|
ENSP00000312352.6:n.*1362T>G
|
|
ENST00000235372.11:c.*1362T>G
|
ENSP00000235372.6:n.*1362T>G
|
|
ENST00000376048.9:c.*1313T>G
|
ENSP00000365216.5:n.*1313T>G
|
|
NM_001135610.1:c.*1313T>G
|
NP_001129082.1:n.*1313T>G
|
|
NM_012231.4:c.*1362T>G
|
NP_036363.2:n.*1362T>G
|
|
XM_011542092.1:c.*1313T>G
|
XP_011540394.1:n.*1313T>G
|
|
XM_011542093.1:c.*1313T>G
|
XP_011540395.1:n.*1313T>G
|
|
XM_017002255.1:c.*1362T>G
|
XP_016857744.1:n.*1362T>G
|
|
XM_017002256.1:c.*1362T>G
|
XP_016857745.1:n.*1362T>G
|
|
XM_017002259.2:c.*1362T>G
|
XP_016857748.1:n.*1362T>G
|
|
XM_017002260.2:c.*1362T>G
|
XP_016857749.1:n.*1362T>G
|
|
XM_017002261.2:c.*1362T>G
|
XP_016857750.1:n.*1362T>G
|
|
XM_017002263.2:c.*1362T>G
|
XP_016857752.1:n.*1362T>G
|
|
XM_017002264.2:c.*1313T>G
|
XP_016857753.1:n.*1313T>G
|
|
XR_002957562.1:n.6349T>G
|
|
|
NM_001135610.2:c.*1313T>G
|
NP_001129082.1:n.*1313T>G
|
|
NM_001393986.1:c.*1362T>G
MANE Select
|
NP_001380915.1:n.*1362T>G
|
|
NM_001393987.1:c.*1362T>G
|
NP_001380916.1:n.*1362T>G
|
|
NM_012231.5:c.*1362T>G
|
NP_036363.2:n.*1362T>G
|
|