ENST00000265631.10:c.884C>A
MANE Select
|
ENSP00000265631.6:p.Pro295His
|
|
ENST00000265631.9:c.884C>A
|
ENSP00000265631.5:p.Pro295His
|
|
ENST00000416240.6:c.884C>A
|
ENSP00000400101.2:p.Pro295His
|
|
ENST00000484495.5:n.37C>A
|
|
|
NM_001160210.1:c.884C>A
|
NP_001153682.1:p.Pro295His
|
|
NM_014251.2:c.884C>A
|
NP_055066.1:p.Pro295His
|
|
NR_027662.1:n.959C>A
|
|
|
XM_006715831.2:c.917C>A
|
XP_006715894.1:p.Pro306His
|
|
XM_011515727.1:c.917C>A
|
XP_011514029.1:p.Pro306His
|
|
XM_011515728.1:c.32C>A
|
XP_011514030.1:p.Pro11His
|
|
XM_006715831.4:c.917C>A
|
XP_006715894.1:p.Pro306His
|
|
XM_011515727.3:c.917C>A
|
XP_011514029.1:p.Pro306His
|
|
XM_017011663.1:c.875C>A
|
XP_016867152.1:p.Pro292His
|
|
XM_017011664.2:c.32C>A
|
XP_016867153.1:p.Pro11His
|
|
XM_017011665.1:c.32C>A
|
XP_016867154.1:p.Pro11His
|
|
XR_001744525.2:n.1055C>A
|
|
|
XR_002956405.1:n.1197C>A
|
|
|
NM_014251.3:c.884C>A
MANE Select
|
NP_055066.1:p.Pro295His
|
|
NR_027662.2:n.910C>A
|
|
|
NM_001160210.2:c.884C>A
|
NP_001153682.1:p.Pro295His
|
|