ENST00000247933.9:c.762G>T
|
ENSP00000247933.4:p.Val254=
|
|
ENST00000514224.2:c.762G>T
MANE Select
|
ENSP00000425081.2:p.Val254=
|
|
ENST00000652070.1:n.818G>T
|
|
|
ENST00000247933.8:c.762G>T
|
ENSP00000247933.4:p.Val254=
|
|
ENST00000502910.5:c.621G>T
|
ENSP00000422952.1:p.Val207=
|
|
ENST00000514192.5:c.579G>T
|
ENSP00000423685.1:p.Val193=
|
|
ENST00000514224.1:c.366G>T
|
ENSP00000425081.1:p.Val122=
|
|
ENST00000514698.5:n.662G>T
|
|
|
NM_000203.4:c.762G>T
|
NP_000194.2:p.Val254=
|
|
NR_110313.1:n.850G>T
|
|
|
XM_006713882.2:c.366G>T
|
XP_006713945.1:p.Val122=
|
|
XM_011513459.1:c.621G>T
|
XP_011511761.1:p.Val207=
|
|
XM_011513460.1:c.621G>T
|
XP_011511762.1:p.Val207=
|
|
XM_011513461.1:c.555G>T
|
XP_011511763.1:p.Val185=
|
|
XM_011513462.1:c.474G>T
|
XP_011511764.1:p.Val158=
|
|
XM_011513463.1:c.474G>T
|
XP_011511765.1:p.Val158=
|
|
XR_924947.1:n.831G>T
|
|
|
NM_000203.5:c.762G>T
MANE Select
|
NP_000194.2:p.Val254=
|
|
NM_001363576.1:c.366G>T
|
NP_001350505.1:p.Val122=
|
|
XM_011513461.2:c.555G>T
|
XP_011511763.1:p.Val185=
|
|
XM_017008163.1:c.-199G>T
|
XP_016863652.1:n.-199G>T
|
|