ENST00000534624.6:c.1194T>C
MANE Select
|
ENSP00000432083.1:p.Pro398=
|
|
ENST00000227378.7:c.1194T>C
|
ENSP00000227378.3:p.Pro398=
|
|
ENST00000453788.6:c.1194T>C
|
ENSP00000404372.2:p.Pro398=
|
|
ENST00000524552.5:c.-34T>C
|
ENSP00000435908.1:n.-34T>C
|
|
ENST00000526110.5:c.1137T>C
|
ENSP00000433584.1:p.Pro379=
|
|
ENST00000526862.1:n.472T>C
|
|
|
ENST00000532091.1:n.941T>C
|
|
|
ENST00000532636.5:c.1194T>C
|
ENSP00000437125.1:p.Pro398=
|
|
ENST00000533238.5:n.381-85T>C
|
|
|
ENST00000533540.5:c.756T>C
|
ENSP00000437189.1:p.Pro252=
|
|
ENST00000534319.5:c.486T>C
|
ENSP00000433316.1:p.Pro162=
|
|
ENST00000534624.5:c.1194T>C
|
ENSP00000432083.1:p.Pro398=
|
|
NM_006597.5:c.1194T>C
|
NP_006588.1:p.Pro398=
|
|
NM_153201.3:c.1194T>C
|
NP_694881.1:p.Pro398=
|
|
XM_011542798.1:c.1194T>C
|
XP_011541100.1:p.Pro398=
|
|
NM_006597.6:c.1194T>C
MANE Select
|
NP_006588.1:p.Pro398=
|
|
NM_153201.4:c.1194T>C
|
NP_694881.1:p.Pro398=
|
|