ENST00000526209.2:c.296C>G
|
|
|
ENST00000681974.1:n.998C>G
|
|
|
ENST00000682693.1:n.1960C>G
|
|
|
ENST00000682886.1:n.496C>G
|
|
|
ENST00000683543.2:c.16374C>G
|
ENSP00000506726.1:p.Ile5458Met
|
|
ENST00000683988.1:c.297C>G
|
ENSP00000506939.1:p.Ile99Met
|
|
ENST00000684428.1:c.861C>G
|
ENSP00000507433.1:p.Ile287Met
|
|
ENST00000684755.1:n.909C>G
|
|
|
ENST00000685024.1:c.1480C>G
|
|
|
ENST00000685166.1:c.16335C>G
|
ENSP00000509386.1:p.Ile5445Met
|
|
ENST00000688411.1:c.803C>G
|
ENSP00000510146.1:n.803C>G
|
|
ENST00000691932.1:c.327C>G
|
ENSP00000509037.1:p.Ile109Met
|
|
ENST00000692637.1:c.16323C>G
|
ENSP00000509666.1:p.Ile5441Met
|
|
ENST00000301067.12:c.16326C>G
MANE Select
|
ENSP00000301067.7:p.Ile5442Met
|
|
ENST00000301067.11:c.16326C>G
|
ENSP00000301067.7:p.Ile5442Met
|
|
ENST00000526209.1:c.369C>G
|
ENSP00000435714.1:p.Ile123Met
|
|
NM_003482.3:c.16326C>G
|
NP_003473.3:p.Ile5442Met
|
|
XM_005269162.3:c.16326C>G
|
XP_005269219.1:p.Ile5442Met
|
|
XM_006719614.2:c.16335C>G
|
XP_006719677.1:p.Ile5445Met
|
|
XM_006719616.2:c.16323C>G
|
XP_006719679.1:p.Ile5441Met
|
|
XM_011538770.1:c.16383C>G
|
XP_011537072.1:p.Ile5461Met
|
|
XM_011538771.1:c.16380C>G
|
XP_011537073.1:p.Ile5460Met
|
|
XM_011538772.1:c.16374C>G
|
XP_011537074.1:p.Ile5458Met
|
|
XM_011538773.1:c.16371C>G
|
XP_011537075.1:p.Ile5457Met
|
|
XM_011538774.1:c.16362C>G
|
XP_011537076.1:p.Ile5454Met
|
|
XM_011538775.1:c.16317C>G
|
XP_011537077.1:p.Ile5439Met
|
|
XM_011538776.1:c.16290C>G
|
XP_011537078.1:p.Ile5430Met
|
|
XM_005269162.4:c.16326C>G
|
XP_005269219.1:p.Ile5442Met
|
|
XM_006719614.4:c.16335C>G
|
XP_006719677.1:p.Ile5445Met
|
|
XM_006719616.3:c.16323C>G
|
XP_006719679.1:p.Ile5441Met
|
|
XM_011538770.2:c.16383C>G
|
XP_011537072.1:p.Ile5461Met
|
|
XM_011538771.2:c.16380C>G
|
XP_011537073.1:p.Ile5460Met
|
|
XM_011538772.2:c.16374C>G
|
XP_011537074.1:p.Ile5458Met
|
|
XM_011538773.2:c.16371C>G
|
XP_011537075.1:p.Ile5457Met
|
|
XM_011538774.2:c.16362C>G
|
XP_011537076.1:p.Ile5454Met
|
|
XM_011538776.2:c.16290C>G
|
XP_011537078.1:p.Ile5430Met
|
|
XR_001748874.1:n.16503C>G
|
|
|
NM_003482.4:c.16326C>G
MANE Select
|
NP_003473.3:p.Ile5442Met
|
|