ENST00000348729.8:c.892G>T
MANE Select
|
ENSP00000302701.4:p.Ala298Ser
|
|
ENST00000348729.7:c.892G>T
|
ENSP00000302701.4:p.Ala298Ser
|
|
ENST00000353963.7:c.904G>T
|
ENSP00000302851.5:p.Ala302Ser
|
|
ENST00000504513.1:c.164+245G>T
|
|
|
ENST00000506512.1:n.503G>T
|
|
|
NM_005847.4:c.892G>T
|
NP_005838.3:p.Ala298Ser
|
|
NM_152685.3:c.904G>T
|
NP_689898.2:p.Ala302Ser
|
|
XM_005272148.3:c.1012G>T
|
XP_005272205.3:p.Ala338Ser
|
|
XM_005272149.3:c.1000G>T
|
XP_005272206.3:p.Ala334Ser
|
|
XM_006714741.2:c.1012G>T
|
XP_006714804.2:p.Ala338Ser
|
|
XM_011543765.1:c.1012G>T
|
XP_011542067.1:p.Ala338Ser
|
|
XM_011543766.1:c.793G>T
|
XP_011542068.1:p.Ala265Ser
|
|
XM_011543767.1:c.697G>T
|
XP_011542069.1:p.Ala233Ser
|
|
XM_011543768.1:c.577G>T
|
XP_011542070.1:p.Ala193Ser
|
|
XM_011543769.1:c.187G>T
|
XP_011542071.1:p.Ala63Ser
|
|
XM_005272149.4:c.1000G>T
|
XP_005272206.3:p.Ala334Ser
|
|
XM_011543765.2:c.1012G>T
|
XP_011542067.1:p.Ala338Ser
|
|
NM_005847.5:c.892G>T
MANE Select
|
NP_005838.3:p.Ala298Ser
|
|
NM_152685.4:c.904G>T
|
NP_689898.2:p.Ala302Ser
|
|