ENST00000426151.7:c.1257G>C
MANE Select
|
ENSP00000389295.1:p.Arg419Ser
|
|
ENST00000649521.1:c.1305G>C
|
ENSP00000497687.1:p.Arg435Ser
|
|
ENST00000359558.6:c.1359G>C
|
ENSP00000352561.2:p.Arg453Ser
|
|
ENST00000360249.8:c.*767G>C
|
ENSP00000353385.5:n.*767G>C
|
|
ENST00000394441.5:c.1257G>C
|
ENSP00000377959.1:p.Arg419Ser
|
|
ENST00000415529.2:c.1307G>C
|
ENSP00000413179.1:n.1307G>C
|
|
ENST00000421592.5:c.1305G>C
|
ENSP00000399552.1:p.Arg435Ser
|
|
ENST00000423724.5:c.1355G>C
|
ENSP00000391369.1:n.1355G>C
|
|
ENST00000426151.5:c.1257G>C
|
ENSP00000389295.1:p.Arg419Ser
|
|
NM_001164737.1:c.1359G>C
|
NP_001158209.1:p.Arg453Ser
|
|
NM_001164738.1:c.1257G>C
|
NP_001158210.1:p.Arg419Ser
|
|
NM_001742.3:c.1257G>C
|
NP_001733.1:p.Arg419Ser
|
|
NM_001164737.2:c.1305G>C
|
NP_001158209.2:p.Arg435Ser
|
|
NM_001742.4:c.1257G>C
MANE Select
|
NP_001733.1:p.Arg419Ser
|
|
NM_001164737.3:c.1305G>C
|
NP_001158209.2:p.Arg435Ser
|
|
NM_001164738.2:c.1257G>C
|
NP_001158210.1:p.Arg419Ser
|
|