ENST00000225964.10:c.4350A>C
MANE Select
|
ENSP00000225964.6:p.Pro1450=
|
|
ENST00000225964.9:c.4350A>C
|
ENSP00000225964.5:p.Pro1450=
|
|
NM_000088.3:c.4350A>C , LRG_1t1:c.4350A>C
|
NP_000079.2:p.Pro1450=
|
|
XM_005257058.3:c.4080A>C
|
XP_005257115.2:p.Pro1360=
|
|
XM_005257059.3:c.3432A>C
|
XP_005257116.2:p.Pro1144=
|
|
XM_011524341.1:c.4152A>C
|
XP_011522643.1:p.Pro1384=
|
|
XM_005257058.4:c.4080A>C
|
XP_005257115.2:p.Pro1360=
|
|
XM_005257059.4:c.3432A>C
|
XP_005257116.2:p.Pro1144=
|
|
NM_000088.4:c.4350A>C
MANE Select
|
NP_000079.2:p.Pro1450=
|
|