ENST00000366647.9:c.595G>A
MANE Select
|
ENSP00000355607.4:p.Glu199Lys
|
|
ENST00000644483.1:c.*281G>A
|
ENSP00000496537.1:n.*281G>A
|
|
ENST00000366647.8:c.595G>A
|
ENSP00000355607.4:p.Glu199Lys
|
|
ENST00000416000.1:c.565G>A
|
ENSP00000411640.1:p.Glu189Lys
|
|
ENST00000436239.5:c.412G>A
|
ENSP00000402811.1:p.Glu138Lys
|
|
NM_001316350.1:c.412G>A
|
NP_001303279.1:p.Glu138Lys
|
|
NM_014236.3:c.595G>A
|
NP_055051.1:p.Glu199Lys
|
|
XM_005273313.3:c.592G>A
|
XP_005273370.1:p.Glu198Lys
|
|
XM_011544303.1:c.268G>A
|
XP_011542605.1:p.Glu90Lys
|
|
XM_011544304.1:c.268G>A
|
XP_011542606.1:p.Glu90Lys
|
|
XM_005273313.4:c.592G>A
|
XP_005273370.1:p.Glu198Lys
|
|
XM_011544303.3:c.268G>A
|
XP_011542605.1:p.Glu90Lys
|
|
XM_011544304.2:c.268G>A
|
XP_011542606.1:p.Glu90Lys
|
|
NM_014236.4:c.595G>A
MANE Select
|
NP_055051.1:p.Glu199Lys
|
|
NM_001316350.2:c.412G>A
|
NP_001303279.1:p.Glu138Lys
|
|