ENST00000324856.13:c.57G>A
MANE Select
|
ENSP00000320485.7:p.Pro19=
|
|
ENST00000430799.7:c.-13+2843G>A
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ENSP00000390317.3:n.-13+2843G>A
|
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ENST00000637465.1:c.-13+360G>A
|
ENSP00000490650.1:n.-13+360G>A
|
|
ENST00000324856.11:c.57G>A
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ENSP00000320485.7:p.Pro19=
|
|
ENST00000457599.6:c.57G>A
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ENSP00000387636.2:p.Pro19=
|
|
NM_006015.4:c.57G>A , LRG_875t1:c.57G>A
|
NP_006006.3:p.Pro19=
|
|
NM_139135.2:c.57G>A
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NP_624361.1:p.Pro19=
|
|
NM_006015.5:c.57G>A
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NP_006006.3:p.Pro19=
|
|
NM_139135.3:c.57G>A
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NP_624361.1:p.Pro19=
|
|
NM_006015.6:c.57G>A
MANE Select
|
NP_006006.3:p.Pro19=
|
|
NM_139135.4:c.57G>A
|
NP_624361.1:p.Pro19=
|
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