ENST00000389048.8:c.3536T>G
MANE Select
|
ENSP00000373700.3:p.Ile1179Ser
|
|
ENST00000431873.6:c.763T>G
|
|
|
ENST00000638605.1:n.413T>G
|
|
|
ENST00000642122.1:c.332T>G
|
ENSP00000493203.1:p.Ile111Ser
|
|
ENST00000389048.7:c.3536T>G
|
ENSP00000373700.3:p.Ile1179Ser
|
|
ENST00000431873.5:c.416T>G
|
ENSP00000414027.2:p.Ile139Ser
|
|
ENST00000618119.4:c.2405T>G
|
ENSP00000482733.1:p.Ile802Ser
|
|
NM_004304.4:c.3536T>G
|
NP_004295.2:p.Ile1179Ser
|
|
NM_001353765.1:c.332T>G
|
NP_001340694.1:p.Ile111Ser
|
|
XM_024452778.1:c.689T>G
|
XP_024308546.1:p.Ile230Ser
|
|
XM_024452779.1:c.332T>G
|
XP_024308547.1:p.Ile111Ser
|
|
NM_004304.5:c.3536T>G
MANE Select
|
NP_004295.2:p.Ile1179Ser
|
|
NM_001353765.2:c.332T>G
|
NP_001340694.1:p.Ile111Ser
|
|