ENST00000262493.12:c.779T>C
MANE Select
|
ENSP00000262493.6:p.Phe260Ser
|
|
ENST00000562316.6:c.446T>C
|
ENSP00000457238.2:p.Phe149Ser
|
|
ENST00000564727.2:c.83T>C
|
ENSP00000454971.2:p.Phe28Ser
|
|
ENST00000568375.2:c.116-3427T>C
|
|
|
ENST00000638185.1:n.994T>C
|
|
|
ENST00000638210.1:n.1079T>C
|
|
|
ENST00000638705.1:c.779T>C
|
ENSP00000491223.1:p.Phe260Ser
|
|
ENST00000638836.1:n.689T>C
|
|
|
ENST00000639055.1:n.1500T>C
|
|
|
ENST00000639251.1:n.680T>C
|
|
|
ENST00000639268.1:c.414T>C
|
|
|
ENST00000639341.1:c.304T>C
|
|
|
ENST00000639770.1:c.817T>C
|
ENSP00000491999.1:n.817T>C
|
|
ENST00000640390.1:n.709T>C
|
|
|
ENST00000640469.1:c.143T>C
|
ENSP00000491875.1:p.Phe48Ser
|
|
ENST00000640560.1:n.555T>C
|
|
|
ENST00000640893.1:c.*177T>C
|
ENSP00000492677.1:n.*177T>C
|
|
ENST00000262493.10:c.779T>C
|
ENSP00000262493.6:p.Phe260Ser
|
|
ENST00000568375.1:n.116-3427T>C
|
|
|
NM_020988.2:c.779T>C
|
NP_066268.1:p.Phe260Ser
|
|
XM_011523003.1:c.653T>C
|
XP_011521305.1:p.Phe218Ser
|
|
XM_011523003.3:c.653T>C
|
XP_011521305.1:p.Phe218Ser
|
|
NM_020988.3:c.779T>C
MANE Select
|
NP_066268.1:p.Phe260Ser
|
|