ENST00000623535.2:c.2679C>T
MANE Select
|
ENSP00000485244.1:p.Pro893=
|
|
ENST00000674046.1:c.2802C>T
|
ENSP00000501174.1:p.Pro934=
|
|
ENST00000379989.6:c.2679C>T
|
ENSP00000369325.3:p.Pro893=
|
|
ENST00000379996.7:c.2679C>T
|
ENSP00000369332.3:p.Pro893=
|
|
ENST00000623535.1:c.2679C>T
|
ENSP00000485244.1:p.Pro893=
|
|
NM_001037343.1:c.2679C>T
|
NP_001032420.1:p.Pro893=
|
|
NM_003159.2:c.2679C>T
|
NP_003150.1:p.Pro893=
|
|
XM_011545569.1:c.2751C>T
|
XP_011543871.1:p.Pro917=
|
|
XM_011545570.1:c.2670C>T
|
XP_011543872.1:p.Pro890=
|
|
XR_950484.1:n.3054C>T
|
|
|
NM_001323289.1:c.2679C>T
|
NP_001310218.1:p.Pro893=
|
|
NM_001323289.2:c.2679C>T
MANE Select
|
NP_001310218.1:p.Pro893=
|
|
NM_001037343.2:c.2679C>T
|
NP_001032420.1:p.Pro893=
|
|
NM_003159.3:c.2679C>T
|
NP_003150.1:p.Pro893=
|
|