ENST00000268070.9:c.2551C>T
MANE Select
|
ENSP00000268070.4:p.Pro851Ser
|
|
ENST00000568565.2:c.2632C>T
|
ENSP00000456161.2:p.Pro878Ser
|
|
ENST00000268070.8:c.2551C>T
|
ENSP00000268070.4:p.Pro851Ser
|
|
NM_139057.2:c.2551C>T
|
NP_620688.2:p.Pro851Ser
|
|
XM_005254872.2:c.2632C>T
|
XP_005254929.1:p.Pro878Ser
|
|
XM_011521312.1:c.2701C>T
|
XP_011519614.1:p.Pro901Ser
|
|
NM_139057.3:c.2551C>T
|
NP_620688.2:p.Pro851Ser
|
|
XM_005254872.3:c.2632C>T
|
XP_005254929.1:p.Pro878Ser
|
|
XM_011521312.2:c.2701C>T
|
XP_011519614.1:p.Pro901Ser
|
|
XM_017021973.2:c.2833C>T
|
XP_016877462.1:p.Pro945Ser
|
|
XM_017021974.1:c.2833C>T
|
XP_016877463.1:p.Pro945Ser
|
|
XM_017021975.1:c.2764C>T
|
XP_016877464.1:p.Pro922Ser
|
|
XM_017021976.1:c.2104C>T
|
XP_016877465.1:p.Pro702Ser
|
|
XM_017021978.1:c.1735C>T
|
XP_016877467.1:p.Pro579Ser
|
|
XM_017021979.1:c.1513C>T
|
XP_016877468.1:p.Pro505Ser
|
|
XM_017021980.1:c.1513C>T
|
XP_016877469.1:p.Pro505Ser
|
|
XM_017021982.1:c.1222C>T
|
XP_016877471.1:p.Pro408Ser
|
|
XM_017021983.1:c.1006C>T
|
XP_016877472.1:p.Pro336Ser
|
|
NM_139057.4:c.2551C>T
MANE Select
|
NP_620688.2:p.Pro851Ser
|
|