ENST00000684169.1:c.712C>T
|
ENSP00000506849.1:p.Pro238Ser
|
|
ENST00000392386.8:c.712C>T
MANE Select
|
ENSP00000376188.2:p.Pro238Ser
|
|
ENST00000392386.7:c.712C>T
|
ENSP00000376188.2:p.Pro238Ser
|
|
ENST00000597131.1:c.177C>T
|
|
|
NM_004750.4:c.712C>T
|
NP_004741.1:p.Pro238Ser
|
|
XM_011528422.1:c.646C>T
|
XP_011526724.1:p.Pro216Ser
|
|
XM_011528423.1:c.712C>T
|
XP_011526725.1:p.Pro238Ser
|
|
XM_011528424.1:c.646C>T
|
XP_011526726.1:p.Pro216Ser
|
|
XM_011528422.2:c.646C>T
|
XP_011526724.1:p.Pro216Ser
|
|
XM_011528423.2:c.712C>T
|
XP_011526725.1:p.Pro238Ser
|
|
XM_011528424.3:c.646C>T
|
XP_011526726.1:p.Pro216Ser
|
|
NM_004750.5:c.712C>T
MANE Select
|
NP_004741.1:p.Pro238Ser
|
|