ENST00000436784.7:c.1031T>C
MANE Select
|
ENSP00000389175.2:p.Met344Thr
|
|
ENST00000305690.12:c.*150T>C
|
ENSP00000301965.9:n.*150T>C
|
|
ENST00000436784.6:c.1031T>C
|
ENSP00000389175.2:p.Met344Thr
|
|
ENST00000461183.5:c.763+16T>C
|
ENSP00000417264.1:n.763+16T>C
|
|
ENST00000471180.5:c.634+16T>C
|
ENSP00000417526.1:n.634+16T>C
|
|
ENST00000473032.5:c.530-461T>C
|
ENSP00000418951.1:n.530-461T>C
|
|
ENST00000477382.1:c.*150T>C
|
ENSP00000419008.1:n.*150T>C
|
|
ENST00000486393.5:c.*394T>C
|
ENSP00000419868.1:n.*394T>C
|
|
ENST00000489173.1:n.1325T>C
|
|
|
NM_001144951.1:c.*150T>C
|
NP_001138423.1:n.*150T>C
|
|
NM_145262.3:c.1031T>C
|
NP_660305.2:p.Met344Thr
|
|
NR_026699.1:n.1129T>C
|
|
|
NR_026700.1:n.695+16T>C
|
|
|
NR_026701.1:n.1127T>C
|
|
|
NR_026702.1:n.626-461T>C
|
|
|
XM_005264878.2:c.*150T>C
|
XP_005264935.1:n.*150T>C
|
|
XR_245095.2:n.2742+16T>C
|
|
|
XM_017005730.1:c.650T>C
|
XP_016861219.1:p.Met217Thr
|
|
XM_024453351.1:c.1031T>C
|
XP_024309119.1:p.Met344Thr
|
|
XM_024453352.1:c.*150T>C
|
XP_024309120.1:n.*150T>C
|
|
XR_001740022.2:n.2933T>C
|
|
|
XR_001740023.2:n.2917+16T>C
|
|
|
XR_245095.4:n.2743+16T>C
|
|
|
NM_145262.4:c.1031T>C
MANE Select
|
NP_660305.2:p.Met344Thr
|
|
NR_026699.2:n.1121T>C
|
|
|
NR_026700.2:n.687+16T>C
|
|
|
NR_026701.2:n.1119T>C
|
|
|
NR_026702.2:n.618-461T>C
|
|
|
NM_001144951.2:c.*150T>C
|
NP_001138423.1:n.*150T>C
|
|