ENST00000225964.10:c.4313C>A
MANE Select
|
ENSP00000225964.6:p.Pro1438His
|
|
ENST00000225964.9:c.4313C>A
|
ENSP00000225964.5:p.Pro1438His
|
|
NM_000088.3:c.4313C>A , LRG_1t1:c.4313C>A
|
NP_000079.2:p.Pro1438His
|
|
XM_005257058.3:c.4043C>A
|
XP_005257115.2:p.Pro1348His
|
|
XM_005257059.3:c.3395C>A
|
XP_005257116.2:p.Pro1132His
|
|
XM_011524341.1:c.4115C>A
|
XP_011522643.1:p.Pro1372His
|
|
XM_005257058.4:c.4043C>A
|
XP_005257115.2:p.Pro1348His
|
|
XM_005257059.4:c.3395C>A
|
XP_005257116.2:p.Pro1132His
|
|
NM_000088.4:c.4313C>A
MANE Select
|
NP_000079.2:p.Pro1438His
|
|