ENST00000257290.10:c.1926G>A
MANE Select
|
ENSP00000257290.5:p.Met642Ile
|
|
ENST00000257290.9:c.1926G>A
|
ENSP00000257290.5:p.Met642Ile
|
|
ENST00000461294.2:n.164G>A
|
|
|
ENST00000507166.5:c.1206G>A
|
ENSP00000423325.1:p.Met402Ile
|
|
ENST00000507536.1:n.352G>A
|
|
|
ENST00000509092.5:n.1744G>A
|
|
|
ENST00000509490.5:c.1926G>A
|
ENSP00000424218.1:p.Met642Ile
|
|
NM_006206.4:c.1926G>A , LRG_309t1:c.1926G>A
|
NP_006197.1:p.Met642Ile
|
|
XM_005265743.1:c.1926G>A
|
XP_005265800.1:p.Met642Ile
|
|
XM_006714039.2:c.2001G>A
|
XP_006714102.1:p.Met667Ile
|
|
XM_006714041.2:c.2001G>A
|
XP_006714104.1:p.Met667Ile
|
|
XM_011534385.1:c.1926G>A
|
XP_011532687.1:p.Met642Ile
|
|
XM_011534386.1:c.1926G>A
|
XP_011532688.1:p.Met642Ile
|
|
NM_001347827.1:c.1926G>A
|
NP_001334756.1:p.Met642Ile
|
|
NM_001347828.1:c.2001G>A
|
NP_001334757.1:p.Met667Ile
|
|
NM_001347829.1:c.1926G>A
|
NP_001334758.1:p.Met642Ile
|
|
NM_001347830.1:c.1965G>A
|
NP_001334759.1:p.Met655Ile
|
|
NM_006206.5:c.1926G>A
|
NP_006197.1:p.Met642Ile
|
|
XM_006714041.3:c.2001G>A
|
XP_006714104.1:p.Met667Ile
|
|
XM_017008281.1:c.1965G>A
|
XP_016863770.1:p.Met655Ile
|
|
NM_006206.6:c.1926G>A
MANE Select
|
NP_006197.1:p.Met642Ile
|
|
NM_001347827.2:c.1926G>A
|
NP_001334756.1:p.Met642Ile
|
|
NM_001347828.2:c.2001G>A
|
NP_001334757.1:p.Met667Ile
|
|
NM_001347829.2:c.1926G>A
|
NP_001334758.1:p.Met642Ile
|
|
NM_001347830.2:c.1965G>A
|
NP_001334759.1:p.Met655Ile
|
|