ENST00000397545.9:c.2721T>C
MANE Select
|
ENSP00000380679.4:p.Ile907=
|
|
ENST00000374877.7:c.2721T>C
|
ENSP00000364011.3:p.Ile907=
|
|
ENST00000397545.8:c.2721T>C
|
ENSP00000380679.4:p.Ile907=
|
|
ENST00000572253.5:n.2972T>C
|
|
|
ENST00000573903.1:n.383T>C
|
|
|
ENST00000574799.5:n.2258T>C
|
|
|
ENST00000575431.1:n.365T>C
|
|
|
NM_001243342.1:c.2721T>C
|
NP_001230271.1:p.Ile907=
|
|
NM_017950.3:c.2721T>C
|
NP_060420.2:p.Ile907=
|
|
XM_011524963.1:c.2631T>C
|
XP_011523265.1:p.Ile877=
|
|
XM_011524964.1:c.1542T>C
|
XP_011523266.1:p.Ile514=
|
|
XR_934495.1:n.2839T>C
|
|
|
XM_011524963.3:c.2631T>C
|
XP_011523265.1:p.Ile877=
|
|
XM_011524964.3:c.1542T>C
|
XP_011523266.1:p.Ile514=
|
|
XM_024450821.1:c.2631T>C
|
XP_024306589.1:p.Ile877=
|
|
XR_934495.2:n.2839T>C
|
|
|
NM_017950.4:c.2721T>C
MANE Select
|
NP_060420.2:p.Ile907=
|
|
NM_001243342.2:c.2721T>C
|
NP_001230271.1:p.Ile907=
|
|