ENST00000288774.8:c.921C>A
|
ENSP00000288774.3:p.Pro307=
|
|
ENST00000447513.7:c.861C>A
MANE Select
|
ENSP00000407922.2:p.Pro287=
|
|
ENST00000650293.1:c.815C>A
|
|
|
ENST00000288774.7:c.921C>A
|
ENSP00000288774.3:p.Pro307=
|
|
ENST00000447513.6:c.861C>A
|
ENSP00000407922.2:p.Pro287=
|
|
ENST00000507596.5:c.861C>A
|
ENSP00000424291.1:p.Pro287=
|
|
ENST00000510434.1:c.*227C>A
|
ENSP00000423051.1:n.*227C>A
|
|
NM_002617.3:c.861C>A
|
NP_002608.1:p.Pro287=
|
|
NM_153818.1:c.921C>A
|
NP_722540.1:p.Pro307=
|
|
XM_011541573.1:c.918C>A
|
XP_011539875.1:p.Pro306=
|
|
XM_011541574.1:c.486C>A
|
XP_011539876.1:p.Pro162=
|
|
XM_011541575.1:c.486C>A
|
XP_011539877.1:p.Pro162=
|
|
XR_946666.1:n.977C>A
|
|
|
XR_946666.2:n.926C>A
|
|
|
NM_001374425.1:c.918C>A
|
NP_001361354.1:p.Pro306=
|
|
NM_001374426.1:c.486C>A
|
NP_001361355.1:p.Pro162=
|
|
NM_001374427.1:c.429C>A
|
NP_001361356.1:p.Pro143=
|
|
NM_002617.4:c.861C>A
MANE Select
|
NP_002608.1:p.Pro287=
|
|
NM_153818.2:c.921C>A
|
NP_722540.1:p.Pro307=
|
|
NR_164636.1:n.976C>A
|
|
|