ENST00000247933.9:c.973-49G>T
|
ENSP00000247933.4:n.973-49G>T
|
|
ENST00000514224.2:c.973-49G>T
MANE Select
|
ENSP00000425081.2:n.973-49G>T
|
|
ENST00000652070.1:n.1029-49G>T
|
|
|
ENST00000247933.8:c.973-49G>T
|
ENSP00000247933.4:n.973-49G>T
|
|
ENST00000514224.1:c.577-49G>T
|
ENSP00000425081.1:n.577-49G>T
|
|
ENST00000514698.5:n.1031G>T
|
|
|
NM_000203.4:c.973-49G>T
|
NP_000194.2:n.973-49G>T
|
|
NR_110313.1:n.1061-49G>T
|
|
|
XM_006713882.2:c.577-49G>T
|
XP_006713945.1:n.577-49G>T
|
|
XM_011513459.1:c.990G>T
|
XP_011511761.1:p.Arg330Ser
|
|
XM_011513460.1:c.832-49G>T
|
XP_011511762.1:n.832-49G>T
|
|
XM_011513461.1:c.766-49G>T
|
XP_011511763.1:n.766-49G>T
|
|
XM_011513462.1:c.685-49G>T
|
XP_011511764.1:n.685-49G>T
|
|
XM_011513463.1:c.685-49G>T
|
XP_011511765.1:n.685-49G>T
|
|
XR_924947.1:n.1042-49G>T
|
|
|
NM_000203.5:c.973-49G>T
MANE Select
|
NP_000194.2:n.973-49G>T
|
|
NM_001363576.1:c.577-49G>T
|
NP_001350505.1:n.577-49G>T
|
|
XM_011513461.2:c.766-49G>T
|
XP_011511763.1:n.766-49G>T
|
|
XM_017008163.1:c.13-49G>T
|
XP_016863652.1:n.13-49G>T
|
|