ENST00000269228.10:c.1025G>C
MANE Select
|
ENSP00000269228.4:p.Trp342Ser
|
|
ENST00000269228.9:c.1025G>C
|
ENSP00000269228.4:p.Trp342Ser
|
|
ENST00000540608.5:n.939G>C
|
|
|
ENST00000591051.1:c.307G>C
|
|
|
NM_000271.4:c.1025G>C
|
NP_000262.2:p.Trp342Ser
|
|
XM_005258277.1:c.1076G>C
|
XP_005258334.1:p.Trp359Ser
|
|
XM_005258278.3:c.1076G>C
|
XP_005258335.1:p.Trp359Ser
|
|
XM_005258279.1:c.1025G>C
|
XP_005258336.1:p.Trp342Ser
|
|
XM_006722479.2:c.1076G>C
|
XP_006722542.1:p.Trp359Ser
|
|
XM_011526015.1:c.611G>C
|
XP_011524317.1:p.Trp204Ser
|
|
XM_005258278.5:c.1076G>C
|
XP_005258335.1:p.Trp359Ser
|
|
XM_005258279.2:c.1025G>C
|
XP_005258336.1:p.Trp342Ser
|
|
XM_006722479.3:c.1076G>C
|
XP_006722542.1:p.Trp359Ser
|
|
XM_017025784.1:c.1076G>C
|
XP_016881273.1:p.Trp359Ser
|
|
XM_017025785.1:c.1076G>C
|
XP_016881274.1:p.Trp359Ser
|
|
XM_017025786.1:c.1025G>C
|
XP_016881275.1:p.Trp342Ser
|
|
XM_017025787.1:c.1025G>C
|
XP_016881276.1:p.Trp342Ser
|
|
NM_000271.5:c.1025G>C
MANE Select
|
NP_000262.2:p.Trp342Ser
|
|