ENST00000347401.8:c.1239G=
|
|
|
ENST00000353578.9:c.7976G=
|
ENSP00000315873.4:p.Ser2659=
|
|
ENST00000682957.1:c.721G=
|
|
|
ENST00000684508.1:n.861G=
|
|
|
ENST00000295550.9:c.8594G=
MANE Select
|
ENSP00000295550.4:p.Ser2865=
|
|
ENST00000295550.8:c.8594G=
|
ENSP00000295550.4:p.Ser2865=
|
|
ENST00000347401.7:c.6770G=
|
ENSP00000315609.4:p.Ser2257=
|
|
ENST00000353578.8:c.7976G=
|
ENSP00000315873.4:p.Ser2659=
|
|
ENST00000409809.5:c.7976G=
|
ENSP00000386844.1:p.Ser2659=
|
|
ENST00000472056.5:c.6773G=
|
ENSP00000418285.1:p.Ser2258=
|
|
ENST00000491769.1:n.5036G=
|
|
|
NM_004369.3:c.8594G= , LRG_473t1:c.8594G=
|
NP_004360.2:p.Ser2865=
|
|
NM_057166.4:c.6773G=
|
NP_476507.3:p.Ser2258=
|
|
NM_057167.3:c.7976G=
|
NP_476508.2:p.Ser2659=
|
|
XM_005246065.1:c.7994G=
|
XP_005246122.1:p.Ser2665=
|
|
XM_005246066.1:c.7373G=
|
XP_005246123.1:p.Ser2458=
|
|
XM_006712253.1:c.8093G=
|
XP_006712316.1:p.Ser2698=
|
|
XM_011510574.1:c.8591G=
|
XP_011508876.1:p.Ser2864=
|
|
XM_011510575.1:c.6188G=
|
XP_011508877.1:p.Ser2063=
|
|
XM_017003304.1:c.6188G=
|
XP_016858793.1:p.Ser2063=
|
|
XM_024452684.1:c.7373G=
|
XP_024308452.1:p.Ser2458=
|
|
NM_004369.4:c.8594G=
MANE Select
|
NP_004360.2:p.Ser2865=
|
|
NM_057166.5:c.6773G=
|
NP_476507.3:p.Ser2258=
|
|
NM_057167.4:c.7976G=
|
NP_476508.2:p.Ser2659=
|
|