ENST00000225964.10:c.4380T>C
MANE Select
|
ENSP00000225964.6:p.Pro1460=
|
|
ENST00000225964.9:c.4380T>C
|
ENSP00000225964.5:p.Pro1460=
|
|
NM_000088.3:c.4380T>C , LRG_1t1:c.4380T>C
|
NP_000079.2:p.Pro1460=
|
|
XM_005257058.3:c.4110T>C
|
XP_005257115.2:p.Pro1370=
|
|
XM_005257059.3:c.3462T>C
|
XP_005257116.2:p.Pro1154=
|
|
XM_011524341.1:c.4182T>C
|
XP_011522643.1:p.Pro1394=
|
|
XM_005257058.4:c.4110T>C
|
XP_005257115.2:p.Pro1370=
|
|
XM_005257059.4:c.3462T>C
|
XP_005257116.2:p.Pro1154=
|
|
NM_000088.4:c.4380T>C
MANE Select
|
NP_000079.2:p.Pro1460=
|
|