ENST00000225964.10:c.387T>G
MANE Select
|
ENSP00000225964.6:p.Pro129=
|
|
ENST00000225964.9:c.387T>G
|
ENSP00000225964.5:p.Pro129=
|
|
ENST00000474644.1:n.608T>G
|
|
|
ENST00000507689.1:c.441T>G
|
ENSP00000460459.1:p.Pro147=
|
|
NM_000088.3:c.387T>G , LRG_1t1:c.387T>G
|
NP_000079.2:p.Pro129=
|
|
XM_005257058.3:c.387T>G
|
XP_005257115.2:p.Pro129=
|
|
XM_005257059.3:c.387T>G
|
XP_005257116.2:p.Pro129=
|
|
XM_011524341.1:c.387T>G
|
XP_011522643.1:p.Pro129=
|
|
XM_005257058.4:c.387T>G
|
XP_005257115.2:p.Pro129=
|
|
XM_005257059.4:c.387T>G
|
XP_005257116.2:p.Pro129=
|
|
NM_000088.4:c.387T>G
MANE Select
|
NP_000079.2:p.Pro129=
|
|