ENST00000436784.7:c.1147A>G
MANE Select
|
ENSP00000389175.2:p.Ile383Val
|
|
ENST00000305690.12:c.*266A>G
|
ENSP00000301965.9:n.*266A>G
|
|
ENST00000436784.6:c.1147A>G
|
ENSP00000389175.2:p.Ile383Val
|
|
ENST00000461183.5:c.763+132A>G
|
ENSP00000417264.1:n.763+132A>G
|
|
ENST00000471180.5:c.634+132A>G
|
ENSP00000417526.1:n.634+132A>G
|
|
ENST00000473032.5:c.530-345A>G
|
ENSP00000418951.1:n.530-345A>G
|
|
ENST00000477382.1:c.*266A>G
|
ENSP00000419008.1:n.*266A>G
|
|
ENST00000486393.5:c.*510A>G
|
ENSP00000419868.1:n.*510A>G
|
|
ENST00000489173.1:n.1441A>G
|
|
|
NM_001144951.1:c.*266A>G
|
NP_001138423.1:n.*266A>G
|
|
NM_145262.3:c.1147A>G
|
NP_660305.2:p.Ile383Val
|
|
NR_026699.1:n.1245A>G
|
|
|
NR_026700.1:n.695+132A>G
|
|
|
NR_026701.1:n.1243A>G
|
|
|
NR_026702.1:n.626-345A>G
|
|
|
XM_005264878.2:c.*266A>G
|
XP_005264935.1:n.*266A>G
|
|
XR_245095.2:n.2742+132A>G
|
|
|
XM_017005730.1:c.766A>G
|
XP_016861219.1:p.Ile256Val
|
|
XM_024453351.1:c.1147A>G
|
XP_024309119.1:p.Ile383Val
|
|
XM_024453352.1:c.*266A>G
|
XP_024309120.1:n.*266A>G
|
|
XR_001740022.2:n.3049A>G
|
|
|
XR_001740023.2:n.2917+132A>G
|
|
|
XR_245095.4:n.2743+132A>G
|
|
|
NM_145262.4:c.1147A>G
MANE Select
|
NP_660305.2:p.Ile383Val
|
|
NR_026699.2:n.1237A>G
|
|
|
NR_026700.2:n.687+132A>G
|
|
|
NR_026701.2:n.1235A>G
|
|
|
NR_026702.2:n.618-345A>G
|
|
|
NM_001144951.2:c.*266A>G
|
NP_001138423.1:n.*266A>G
|
|