ENST00000243964.7:c.3063C>G
MANE Select
|
ENSP00000243964.4:p.Pro1021=
|
|
ENST00000243964.6:c.3063C>G
|
ENSP00000243964.3:p.Pro1021=
|
|
ENST00000454036.6:c.3132C>G
|
ENSP00000387694.1:p.Pro1044=
|
|
ENST00000616201.4:c.1298-2139C>G
|
ENSP00000484585.1:n.1298-2139C>G
|
|
ENST00000616202.4:c.613-1964C>G
|
ENSP00000478369.1:n.613-1964C>G
|
|
ENST00000616933.4:c.*2381C>G
|
ENSP00000477569.1:n.*2381C>G
|
|
ENST00000626937.2:c.510-3082C>G
|
ENSP00000485953.1:n.510-3082C>G
|
|
NM_001134771.1:c.3132C>G
|
NP_001128243.1:p.Pro1044=
|
|
NM_020708.4:c.3063C>G
|
NP_065759.1:p.Pro1021=
|
|
XM_017027981.1:c.3132C>G
|
XP_016883470.1:p.Pro1044=
|
|
NM_001134771.2:c.3132C>G
|
NP_001128243.1:p.Pro1044=
|
|
NM_020708.5:c.3063C>G
MANE Select
|
NP_065759.1:p.Pro1021=
|
|