|
NM_020964.3:c.5514G>T
MANE Select
|
NP_066015.2:p.Met1838Ile
|
|
ENST00000282041.11:c.5514G>T
MANE Select
|
ENSP00000282041.4:p.Met1838Ile
|
|
NM_020964.2:c.5514G>T
|
NP_066015.2:p.Met1838Ile
|
|
ENST00000282041.9:c.5514G>T
|
ENSP00000282041.4:p.Met1838Ile
|
|
ENST00000585906.5:n.2293G>T
|
|
|
ENST00000586655.2:n.3775G>T
|
|
|
ENST00000587884.1:c.*1254G>T
|
ENSP00000466990.1:n.*1254G>T
|
|
ENST00000587884.2:c.5640G>T
|
ENSP00000466990.2:n.5640G>T
|
|
ENST00000587973.2:n.1379G>T
|
|
|
ENST00000590884.5:c.*109G>T
|
ENSP00000466403.1:n.*109G>T
|
|
ENST00000590884.6:c.5458G>T
|
ENSP00000466403.2:n.5458G>T
|
|
ENST00000592272.5:c.2139G>T
|
ENSP00000467464.1:p.Met713Ile
|
|
ENST00000592272.6:c.5514G>T
|
ENSP00000467464.2:p.Met1838Ile
|
|
ENST00000696481.1:n.2146G>T
|
|
|
ENST00000696482.1:c.5254G>T
|
ENSP00000512656.1:n.5254G>T
|
|
ENST00000696483.1:c.5514G>T
|
ENSP00000512657.1:p.Met1838Ile
|
|
ENST00000696484.1:c.5514G>T
|
ENSP00000512658.1:p.Met1838Ile
|
|
ENST00000696485.1:c.*109G>T
|
ENSP00000512659.1:n.*109G>T
|
|
ENST00000696489.1:c.5514G>T
|
ENSP00000512660.1:p.Met1838Ile
|
|
ENST00000696490.1:c.5514G>T
|
ENSP00000512661.1:p.Met1838Ile
|
|
XM_011526120.1:c.5541G>T
|
XP_011524422.1:p.Met1847Ile
|
|
XM_011526121.1:c.5541G>T
|
XP_011524423.1:p.Met1847Ile
|
|
XM_011526122.1:c.5514G>T
|
XP_011524424.1:p.Met1838Ile
|
|
XM_011526123.1:c.5541G>T
|
XP_011524425.1:p.Met1847Ile
|
|
XM_011526124.1:c.5541G>T
|
XP_011524426.1:p.Met1847Ile
|
|
XM_011526125.1:c.5400G>T
|
XP_011524427.1:p.Met1800Ile
|
|
XM_011526126.1:c.4476G>T
|
XP_011524428.1:p.Met1492Ile
|
|
XM_011526127.1:c.5541G>T
|
XP_011524429.1:p.Met1847Ile
|
|
XM_017025889.1:c.5514G>T
|
XP_016881378.1:p.Met1838Ile
|
|
XM_017025890.2:c.5514G>T
|
XP_016881379.1:p.Met1838Ile
|
|
XM_017025891.1:c.5373G>T
|
XP_016881380.1:p.Met1791Ile
|
|
XM_017025892.1:c.4449G>T
|
XP_016881381.1:p.Met1483Ile
|
|
XM_017025893.1:c.2139G>T
|
XP_016881382.1:p.Met713Ile
|
|
XR_001753256.1:n.5596G>T
|
|
|
XR_001753257.1:n.5540G>T
|
|
|
XR_935244.1:n.5614G>T
|
|
