ENST00000403625.7:c.390C>T
MANE Select
|
ENSP00000385727.1:p.Pro130=
|
|
ENST00000403625.6:c.390C>T
|
ENSP00000385727.1:p.Pro130=
|
|
ENST00000406039.5:c.390C>T
|
ENSP00000384547.1:p.Pro130=
|
|
ENST00000406374.5:c.390C>T
|
ENSP00000385088.1:p.Pro130=
|
|
ENST00000432817.5:c.6C>T
|
ENSP00000413573.1:p.Pro2=
|
|
ENST00000452953.5:c.8C>T
|
|
|
ENST00000478569.1:n.254C>T
|
|
|
NM_001164664.1:c.390C>T
|
NP_001158136.1:p.Pro130=
|
|
NM_001290228.1:c.390C>T
|
NP_001277157.1:p.Pro130=
|
|
NM_198828.2:c.390C>T
|
NP_942123.1:p.Pro130=
|
|
XM_011543381.1:c.390C>T
|
XP_011541683.1:p.Pro130=
|
|
XM_011543382.1:c.390C>T
|
XP_011541684.1:p.Pro130=
|
|
XM_011543383.1:c.390C>T
|
XP_011541685.1:p.Pro130=
|
|
XM_024446044.1:c.390C>T
|
XP_024301812.1:p.Pro130=
|
|
NM_001164664.2:c.390C>T
MANE Select
|
NP_001158136.1:p.Pro130=
|
|
NM_001290228.2:c.390C>T
|
NP_001277157.1:p.Pro130=
|
|
NM_198828.3:c.390C>T
|
NP_942123.1:p.Pro130=
|
|
NM_001393524.1:c.390C>T
|
NP_001380453.1:p.Pro130=
|
|
NM_001393525.1:c.390C>T
|
NP_001380454.1:p.Pro130=
|
|