ENST00000328195.8:c.441C>A
MANE Select
|
ENSP00000333551.3:p.Thr147=
|
|
ENST00000328195.7:c.441C>A
|
ENSP00000333551.3:p.Thr147=
|
|
ENST00000521631.1:n.124C>A
|
|
|
ENST00000523187.5:c.285C>A
|
ENSP00000427886.1:p.Thr95=
|
|
ENST00000523358.5:c.441C>A
|
ENSP00000427778.1:p.Thr147=
|
|
ENST00000523521.1:c.198C>A
|
ENSP00000429425.1:p.Thr66=
|
|
NM_007198.3:c.441C>A
|
NP_009129.1:p.Thr147=
|
|
NM_001349346.1:c.441C>A
|
NP_001336275.1:p.Thr147=
|
|
NM_001349347.1:c.435C>A
|
NP_001336276.1:p.Thr145=
|
|
NM_001349348.1:c.285C>A
|
NP_001336277.1:p.Thr95=
|
|
NM_007198.4:c.441C>A
MANE Select
|
NP_009129.1:p.Thr147=
|
|
NM_001349346.2:c.441C>A
|
NP_001336275.1:p.Thr147=
|
|
NM_001349347.2:c.435C>A
|
NP_001336276.1:p.Thr145=
|
|
NM_001349348.2:c.285C>A
|
NP_001336277.1:p.Thr95=
|
|