ENST00000247933.9:c.1085A=
|
ENSP00000247933.4:p.Gln362=
|
|
ENST00000514224.2:c.1085A=
MANE Select
|
ENSP00000425081.2:p.Gln362=
|
|
ENST00000652070.1:n.1141A=
|
|
|
ENST00000247933.8:c.1085A=
|
ENSP00000247933.4:p.Gln362=
|
|
ENST00000514224.1:c.689A=
|
ENSP00000425081.1:p.Gln230=
|
|
ENST00000514698.5:n.1192A=
|
|
|
NM_000203.4:c.1085A=
|
NP_000194.2:p.Gln362=
|
|
NR_110313.1:n.1173A=
|
|
|
XM_006713882.2:c.689A=
|
XP_006713945.1:p.Gln230=
|
|
XM_011513459.1:c.1151A=
|
XP_011511761.1:p.Gln384=
|
|
XM_011513460.1:c.944A=
|
XP_011511762.1:p.Gln315=
|
|
XM_011513461.1:c.878A=
|
XP_011511763.1:p.Gln293=
|
|
XM_011513462.1:c.797A=
|
XP_011511764.1:p.Gln266=
|
|
XM_011513463.1:c.797A=
|
XP_011511765.1:p.Gln266=
|
|
XR_924947.1:n.1154A=
|
|
|
NM_000203.5:c.1085A=
MANE Select
|
NP_000194.2:p.Gln362=
|
|
NM_001363576.1:c.689A=
|
NP_001350505.1:p.Gln230=
|
|
XM_011513461.2:c.878A=
|
XP_011511763.1:p.Gln293=
|
|
XM_017008163.1:c.125A=
|
XP_016863652.1:p.Gln42=
|
|