ENST00000478003.2:n.1898G>A
|
|
|
ENST00000682276.1:n.1515G>A
|
|
|
ENST00000682892.1:c.1617G>A
|
ENSP00000507214.1:p.Met539Ile
|
|
ENST00000682952.1:n.1709G>A
|
|
|
ENST00000684455.1:c.1283G>A
|
|
|
ENST00000684642.1:c.1467G>A
|
ENSP00000507355.1:p.Met489Ile
|
|
ENST00000684740.1:n.2248G>A
|
|
|
ENST00000303236.9:c.2070G>A
MANE Select
|
ENSP00000307235.3:p.Met690Ile
|
|
ENST00000652099.1:c.2264G>A
|
|
|
ENST00000652736.1:n.1946G>A
|
|
|
ENST00000303236.7:c.2070G>A
|
ENSP00000307235.3:p.Met690Ile
|
|
ENST00000415570.1:c.1707G>A
|
ENSP00000412076.1:p.Met569Ile
|
|
ENST00000419748.5:c.1617G>A
|
ENSP00000408325.1:p.Met539Ile
|
|
ENST00000478003.1:n.636G>A
|
|
|
NM_001313915.1:c.1617G>A
|
NP_001300844.1:p.Met539Ile
|
|
NM_004836.5:c.2070G>A
|
NP_004827.4:p.Met690Ile
|
|
NM_004836.6:c.2070G>A
|
NP_004827.4:p.Met690Ile
|
|
NR_110236.1:n.1550C>T
|
|
|
XM_005264649.3:c.1386G>A
|
XP_005264706.1:p.Met462Ile
|
|
XR_939749.1:n.2349G>A
|
|
|
XM_017005376.2:c.1386G>A
|
XP_016860865.1:p.Met462Ile
|
|
NM_004836.7:c.2070G>A
MANE Select
|
NP_004827.4:p.Met690Ile
|
|
NM_001313915.2:c.1617G>A
|
NP_001300844.1:p.Met539Ile
|
|