ENST00000682089.1:n.316G>A
|
|
|
ENST00000682266.1:c.546G>A
|
ENSP00000507766.1:p.Met182Ile
|
|
ENST00000682341.1:c.954G>A
|
ENSP00000508251.1:p.Met318Ile
|
|
ENST00000682530.1:c.*928G>A
|
ENSP00000506805.1:n.*928G>A
|
|
ENST00000683197.1:c.954G>A
|
ENSP00000507641.1:p.Met318Ile
|
|
ENST00000683411.1:c.546G>A
|
ENSP00000508397.1:p.Met182Ile
|
|
ENST00000683437.1:c.546G>A
|
ENSP00000508408.1:p.Met182Ile
|
|
ENST00000683613.1:n.1990G>A
|
|
|
ENST00000683834.1:n.1196G>A
|
|
|
ENST00000684663.1:c.951G>A
|
ENSP00000508009.1:p.Met317Ile
|
|
ENST00000324559.9:c.996G>A
MANE Select
|
ENSP00000315371.9:p.Met332Ile
|
|
ENST00000648804.1:n.1331G>A
|
|
|
ENST00000324559.8:c.996G>A
|
ENSP00000315371.8:p.Met332Ile
|
|
NM_001142649.1:c.993G>A
|
NP_001136121.1:p.Met331Ile
|
|
NM_213599.2:c.996G>A , LRG_868t1:c.996G>A
|
NP_998764.1:p.Met332Ile
|
|
XM_005252820.2:c.954G>A
|
XP_005252877.2:p.Met318Ile
|
|
XM_005252821.2:c.951G>A
|
XP_005252878.2:p.Met317Ile
|
|
XM_005252822.3:c.918G>A
|
XP_005252879.1:p.Met306Ile
|
|
XM_005252823.3:c.915G>A
|
XP_005252880.1:p.Met305Ile
|
|
XM_011519949.1:c.903G>A
|
XP_011518251.1:p.Met301Ile
|
|
XM_005252820.3:c.954G>A
|
XP_005252877.2:p.Met318Ile
|
|
XM_005252821.3:c.951G>A
|
XP_005252878.2:p.Met317Ile
|
|
XM_005252822.4:c.918G>A
|
XP_005252879.1:p.Met306Ile
|
|
XM_011519949.2:c.903G>A
|
XP_011518251.1:p.Met301Ile
|
|
NM_001142649.2:c.993G>A
|
NP_001136121.1:p.Met331Ile
|
|
NM_213599.3:c.996G>A
MANE Select
|
NP_998764.1:p.Met332Ile
|
|