ENST00000369538.4:c.1260C>G
|
ENSP00000358551.4:p.Pro420=
|
|
ENST00000520113.7:c.1272C>G
MANE Select
|
ENSP00000430075.3:p.Pro424=
|
|
ENST00000637080.1:c.1055C>G
|
ENSP00000489753.1:n.1055C>G
|
|
ENST00000639077.1:n.937C>G
|
|
|
ENST00000369538.3:c.1359C>G
|
ENSP00000358551.3:p.Pro453=
|
|
ENST00000520113.6:c.1371C>G
|
ENSP00000430075.2:p.Pro457=
|
|
NM_000036.2:c.1371C>G
|
NP_000027.2:p.Pro457=
|
|
NM_001172626.1:c.1359C>G
|
NP_001166097.1:p.Pro453=
|
|
NM_000036.3:c.1272C>G
MANE Select
|
NP_000027.3:p.Pro424=
|
|
NM_001172626.2:c.1260C>G
|
NP_001166097.2:p.Pro420=
|
|