ENST00000309424.8:c.48C>T
MANE Select
|
ENSP00000310966.3:p.Pro16=
|
|
ENST00000309424.7:c.48C>T
|
ENSP00000310966.3:p.Pro16=
|
|
ENST00000589804.1:c.54C>T
|
ENSP00000465099.1:p.Pro18=
|
|
ENST00000590794.1:c.20+401C>T
|
|
|
ENST00000592852.1:c.-487C>T
|
ENSP00000467771.1:n.-487C>T
|
|
NM_001297590.1:c.54C>T
|
NP_001284519.1:p.Pro18=
|
|
NM_012099.1:c.48C>T
|
NP_036231.1:p.Pro16=
|
|
NM_001297590.2:c.54C>T
|
NP_001284519.1:p.Pro18=
|
|
NM_012099.2:c.48C>T
|
NP_036231.1:p.Pro16=
|
|
NM_001297590.3:c.54C>T
|
NP_001284519.1:p.Pro18=
|
|
NM_012099.3:c.48C>T
MANE Select
|
NP_036231.1:p.Pro16=
|
|