NM_005215.4:c.3931C>T
MANE Select
|
NP_005206.2:p.Pro1311Ser
|
ENST00000442544.7:c.3931C>T
MANE Select
|
ENSP00000389140.2:p.Pro1311Ser
|
NM_005215.3:c.3931C>T
|
NP_005206.2:p.Pro1311Ser
|
ENST00000412726.5:c.3862C>T
|
ENSP00000397322.2:p.Pro1288Ser
|
ENST00000442544.6:c.3931C>T
|
ENSP00000389140.2:p.Pro1311Ser
|
ENST00000579702.1:n.16C>T
|
|
ENST00000581580.5:c.2830C>T
|
ENSP00000464582.1:p.Pro944Ser
|
XM_011525843.1:c.3931C>T
|
XP_011524145.1:p.Pro1311Ser
|
XM_011525844.1:c.2896C>T
|
XP_011524146.1:p.Pro966Ser
|
XM_011525844.2:c.2896C>T
|
XP_011524146.1:p.Pro966Ser
|
XM_017025568.1:c.3925C>T
|
XP_016881057.1:p.Pro1309Ser
|
XM_017025569.1:c.3871C>T
|
XP_016881058.1:p.Pro1291Ser
|
XM_017025570.1:c.2896C>T
|
XP_016881059.1:p.Pro966Ser
|