ENST00000268070.9:c.2553C>G
MANE Select
|
ENSP00000268070.4:p.Pro851=
|
|
ENST00000568565.2:c.2634C>G
|
ENSP00000456161.2:p.Pro878=
|
|
ENST00000268070.8:c.2553C>G
|
ENSP00000268070.4:p.Pro851=
|
|
NM_139057.2:c.2553C>G
|
NP_620688.2:p.Pro851=
|
|
XM_005254872.2:c.2634C>G
|
XP_005254929.1:p.Pro878=
|
|
XM_011521312.1:c.2703C>G
|
XP_011519614.1:p.Pro901=
|
|
NM_139057.3:c.2553C>G
|
NP_620688.2:p.Pro851=
|
|
XM_005254872.3:c.2634C>G
|
XP_005254929.1:p.Pro878=
|
|
XM_011521312.2:c.2703C>G
|
XP_011519614.1:p.Pro901=
|
|
XM_017021973.2:c.2835C>G
|
XP_016877462.1:p.Pro945=
|
|
XM_017021974.1:c.2835C>G
|
XP_016877463.1:p.Pro945=
|
|
XM_017021975.1:c.2766C>G
|
XP_016877464.1:p.Pro922=
|
|
XM_017021976.1:c.2106C>G
|
XP_016877465.1:p.Pro702=
|
|
XM_017021978.1:c.1737C>G
|
XP_016877467.1:p.Pro579=
|
|
XM_017021979.1:c.1515C>G
|
XP_016877468.1:p.Pro505=
|
|
XM_017021980.1:c.1515C>G
|
XP_016877469.1:p.Pro505=
|
|
XM_017021982.1:c.1224C>G
|
XP_016877471.1:p.Pro408=
|
|
XM_017021983.1:c.1008C>G
|
XP_016877472.1:p.Pro336=
|
|
NM_139057.4:c.2553C>G
MANE Select
|
NP_620688.2:p.Pro851=
|
|