ENST00000426263.10:c.844C>T
MANE Select
|
ENSP00000416293.2:p.Gln282Ter
|
|
ENST00000674765.1:c.844C>T
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ENSP00000501811.1:p.Gln282Ter
|
|
ENST00000675112.1:n.867C>T
|
|
|
ENST00000676254.1:n.1293C>T
|
|
|
ENST00000426263.7:c.844C>T
|
ENSP00000416293.2:p.Gln282Ter
|
|
ENST00000439722.2:c.723C>T
|
ENSP00000395521.2:n.723C>T
|
|
ENST00000475162.3:c.415+1010C>T
|
|
|
ENST00000630287.2:c.*159C>T
|
ENSP00000486694.1:n.*159C>T
|
|
NM_006516.2:c.844C>T
|
NP_006507.2:p.Gln282Ter
|
|
NM_006516.3:c.844C>T
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NP_006507.2:p.Gln282Ter
|
|
NM_006516.4:c.844C>T
MANE Select
|
NP_006507.2:p.Gln282Ter
|
|