ENST00000332896.8:c.369G>T
MANE Select
|
ENSP00000327647.3:p.Leu123=
|
|
ENST00000332896.7:c.369G>T
|
ENSP00000327647.3:p.Leu123=
|
|
ENST00000542893.2:c.369G>T
|
ENSP00000439068.2:p.Leu123=
|
|
ENST00000548330.1:n.754G>T
|
|
|
ENST00000548483.5:c.299-44010G>T
|
ENSP00000448685.1:n.299-44010G>T
|
|
ENST00000550030.1:n.169G>T
|
|
|
ENST00000551065.5:c.299-9279G>T
|
ENSP00000448425.1:n.299-9279G>T
|
|
ENST00000609189.1:n.145G>T
|
|
|
NM_003805.3:c.369G>T
|
NP_003796.1:p.Leu123=
|
|
XM_005269211.3:c.299-44010G>T
|
XP_005269268.1:n.299-44010G>T
|
|
NM_001320099.1:c.369G>T
|
NP_001307028.1:p.Leu123=
|
|
NM_001320100.1:c.299-44010G>T
|
NP_001307029.1:n.299-44010G>T
|
|
NM_003805.4:c.369G>T
|
NP_003796.1:p.Leu123=
|
|
NR_135147.1:n.407-9279G>T
|
|
|
XM_017020144.1:c.299-9279G>T
|
XP_016875633.1:n.299-9279G>T
|
|
XR_001748910.1:n.430-9279G>T
|
|
|
NM_003805.5:c.369G>T
MANE Select
|
NP_003796.1:p.Leu123=
|
|
NM_001320099.2:c.369G>T
|
NP_001307028.1:p.Leu123=
|
|
NM_001320100.2:c.299-44010G>T
|
NP_001307029.1:n.299-44010G>T
|
|
NR_135147.2:n.403-9279G>T
|
|
|