ENST00000300900.9:c.12G>C
MANE Select
|
ENSP00000300900.3:p.Leu4=
|
|
ENST00000300900.8:c.12G>C
|
ENSP00000300900.3:p.Leu4=
|
|
ENST00000585705.5:n.105G>C
|
|
|
ENST00000586876.1:c.12G>C
|
ENSP00000467465.1:p.Leu4=
|
|
ENST00000591725.1:c.-347G>C
|
ENSP00000466964.1:n.-347G>C
|
|
NM_000717.3:c.12G>C
|
NP_000708.1:p.Leu4=
|
|
XM_005257639.1:c.12G>C
|
XP_005257696.1:p.Leu4=
|
|
NM_000717.4:c.12G>C
|
NP_000708.1:p.Leu4=
|
|
NR_137422.1:n.111G>C
|
|
|
XM_005257639.3:c.12G>C
|
XP_005257696.1:p.Leu4=
|
|
XR_001752604.2:n.105G>C
|
|
|
XR_001752605.2:n.105G>C
|
|
|
XR_001752606.2:n.105G>C
|
|
|
XR_001752607.2:n.105G>C
|
|
|
XR_001752608.2:n.105G>C
|
|
|
XR_001752609.2:n.105G>C
|
|
|
XR_001752610.2:n.105G>C
|
|
|
NM_000717.5:c.12G>C
MANE Select
|
NP_000708.1:p.Leu4=
|
|
NR_137422.2:n.74G>C
|
|
|