ENST00000329198.5:c.286G>T
MANE Select
|
ENSP00000327758.4:p.Ala96Ser
|
|
ENST00000329198.4:c.286G>T
|
ENSP00000327758.4:p.Ala96Ser
|
|
ENST00000424406.2:c.286G>T
|
ENSP00000395378.2:p.Ala96Ser
|
|
ENST00000517440.1:c.286G>T
|
ENSP00000429905.1:p.Ala96Ser
|
|
ENST00000521848.1:c.286G>T
|
ENSP00000427906.1:p.Ala96Ser
|
|
NM_001166175.1:c.286G>T
|
NP_001159647.1:p.Ala96Ser
|
|
NM_001166176.1:c.286G>T
|
NP_001159648.1:p.Ala96Ser
|
|
NM_004387.3:c.286G>T
|
NP_004378.1:p.Ala96Ser
|
|
XM_017009071.2:c.286G>T
|
XP_016864560.1:p.Ala96Ser
|
|
NM_004387.4:c.286G>T
MANE Select
|
NP_004378.1:p.Ala96Ser
|
|
NM_001166175.2:c.286G>T
|
NP_001159647.1:p.Ala96Ser
|
|
NM_001166176.2:c.286G>T
|
NP_001159648.1:p.Ala96Ser
|
|