ENST00000260197.12:c.2327C>A
MANE Select
|
ENSP00000260197.6:p.Ser776Ter
|
|
ENST00000260197.11:c.2327C>A
|
ENSP00000260197.6:p.Ser776Ter
|
|
NM_003105.5:c.2327C>A
|
NP_003096.1:p.Ser776Ter
|
|
XM_011542963.1:c.2327C>A
|
XP_011541265.1:p.Ser776Ter
|
|
XM_011542964.1:c.2327C>A
|
XP_011541266.1:p.Ser776Ter
|
|
XM_011542965.1:c.788C>A
|
XP_011541267.1:p.Ser263Ter
|
|
XM_011542963.3:c.2327C>A
|
XP_011541265.1:p.Ser776Ter
|
|
XM_011542965.3:c.788C>A
|
XP_011541267.1:p.Ser263Ter
|
|
XM_017018169.2:c.2015C>A
|
XP_016873658.1:p.Ser672Ter
|
|
XM_017018170.2:c.1802C>A
|
XP_016873659.1:p.Ser601Ter
|
|
XM_017018171.1:c.2327C>A
|
XP_016873660.1:p.Ser776Ter
|
|
XM_017018172.2:c.-222C>A
|
XP_016873661.1:n.-222C>A
|
|
NM_003105.6:c.2327C>A
MANE Select
|
NP_003096.2:p.Ser776Ter
|
|