ENST00000297679.10:c.615C>T
MANE Select
|
ENSP00000297679.5:p.Phe205=
|
|
ENST00000262520.10:c.531+219C>T
|
ENSP00000262520.6:n.531+219C>T
|
|
ENST00000297679.9:c.615C>T
|
ENSP00000297679.5:p.Phe205=
|
|
NM_001142777.1:c.531+219C>T
|
NP_001136249.1:n.531+219C>T
|
|
NM_001142778.1:c.531+219C>T
|
NP_001136250.1:n.531+219C>T
|
|
NM_025193.3:c.615C>T
|
NP_079469.2:p.Phe205=
|
|
XM_005255601.3:c.615C>T
|
XP_005255658.2:p.Phe205=
|
|
XM_011545960.1:c.615C>T
|
XP_011544262.1:p.Phe205=
|
|
XM_011545961.1:c.615C>T
|
XP_011544263.1:p.Phe205=
|
|
XM_011545962.1:c.531+219C>T
|
XP_011544264.1:n.531+219C>T
|
|
XM_011545960.2:c.615C>T
|
XP_011544262.1:p.Phe205=
|
|
XM_011545962.2:c.531+219C>T
|
XP_011544264.1:n.531+219C>T
|
|
XM_017023732.1:c.531+219C>T
|
XP_016879221.1:n.531+219C>T
|
|
NM_025193.4:c.615C>T
MANE Select
|
NP_079469.2:p.Phe205=
|
|
NM_001142777.2:c.531+219C>T
|
NP_001136249.1:n.531+219C>T
|
|
NM_001142778.2:c.531+219C>T
|
NP_001136250.1:n.531+219C>T
|
|