ENST00000399220.3:c.387G>A
MANE Select
|
ENSP00000382166.3:p.Leu129=
|
|
ENST00000358309.3:c.483G>A
|
ENSP00000351059.3:p.Leu161=
|
|
ENST00000399220.2:c.387G>A
|
ENSP00000382166.2:p.Leu129=
|
|
ENST00000435290.1:c.387G>A
|
ENSP00000394960.1:p.Leu129=
|
|
ENST00000541347.5:c.387G>A
|
ENSP00000439140.1:p.Leu129=
|
|
ENST00000542107.5:c.387G>A
|
ENSP00000444928.1:p.Leu129=
|
|
NM_001171171.1:c.387G>A
|
NP_001164642.1:p.Leu129=
|
|
NM_001171172.1:c.387G>A
|
NP_001164643.1:p.Leu129=
|
|
NM_001171174.1:c.483G>A
|
NP_001164645.1:p.Leu161=
|
|
NM_001337.3:c.387G>A
|
NP_001328.1:p.Leu129=
|
|
NM_001337.4:c.387G>A
MANE Select
|
NP_001328.1:p.Leu129=
|
|
NM_001171171.2:c.387G>A
|
NP_001164642.1:p.Leu129=
|
|
NM_001171172.2:c.387G>A
|
NP_001164643.1:p.Leu129=
|
|