ENST00000426263.10:c.834G>A
MANE Select
|
ENSP00000416293.2:p.Leu278=
|
|
ENST00000674765.1:c.834G>A
|
ENSP00000501811.1:p.Leu278=
|
|
ENST00000675112.1:n.857G>A
|
|
|
ENST00000676254.1:n.1283G>A
|
|
|
ENST00000426263.7:c.834G>A
|
ENSP00000416293.2:p.Leu278=
|
|
ENST00000439722.2:c.713G>A
|
ENSP00000395521.2:n.713G>A
|
|
ENST00000475162.3:c.415+1000G>A
|
|
|
ENST00000630287.2:c.*149G>A
|
ENSP00000486694.1:n.*149G>A
|
|
NM_006516.2:c.834G>A
|
NP_006507.2:p.Leu278=
|
|
NM_006516.3:c.834G>A
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NP_006507.2:p.Leu278=
|
|
NM_006516.4:c.834G>A
MANE Select
|
NP_006507.2:p.Leu278=
|
|