ENST00000426263.10:c.509T>G
MANE Select
|
ENSP00000416293.2:p.Ile170Ser
|
|
ENST00000674765.1:c.509T>G
|
ENSP00000501811.1:p.Ile170Ser
|
|
ENST00000675112.1:n.532T>G
|
|
|
ENST00000676254.1:n.958T>G
|
|
|
ENST00000426263.7:c.509T>G
|
ENSP00000416293.2:p.Ile170Ser
|
|
ENST00000439722.2:c.388T>G
|
ENSP00000395521.2:n.388T>G
|
|
ENST00000475162.3:c.408T>G
|
|
|
ENST00000625233.2:n.717T>G
|
|
|
ENST00000630287.2:c.509T>G
|
ENSP00000486694.1:p.Ile170Ser
|
|
NM_006516.2:c.509T>G
|
NP_006507.2:p.Ile170Ser
|
|
NM_006516.3:c.509T>G
|
NP_006507.2:p.Ile170Ser
|
|
NM_006516.4:c.509T>G
MANE Select
|
NP_006507.2:p.Ile170Ser
|
|