ENST00000262407.6:c.3054G>C
MANE Select
|
ENSP00000262407.5:p.Met1018Ile
|
|
ENST00000648408.1:c.2374+299G>C
|
|
|
ENST00000262407.5:c.3054G>C
|
ENSP00000262407.5:p.Met1018Ile
|
|
ENST00000587295.5:c.253+1473G>C
|
|
|
ENST00000588098.1:c.37+299G>C
|
|
|
ENST00000592462.5:n.2753G>C
|
|
|
NM_000419.3:c.3054G>C , LRG_479t1:c.3054G>C
|
NP_000410.2:p.Met1018Ile
|
|
XM_011524749.1:c.2952G>C
|
XP_011523051.1:p.Met984Ile
|
|
XM_011524750.1:c.2943+299G>C
|
XP_011523052.1:n.2943+299G>C
|
|
NM_000419.4:c.3054G>C
|
NP_000410.2:p.Met1018Ile
|
|
NM_000419.5:c.3054G>C
MANE Select
|
NP_000410.2:p.Met1018Ile
|
|