ENST00000622290.5:c.2995G>T
|
ENSP00000483331.2:p.Ala999Ser
|
|
ENST00000205557.12:c.2995G>T
MANE Select
|
ENSP00000205557.7:p.Ala999Ser
|
|
ENST00000205557.11:c.2995G>T
|
ENSP00000205557.7:p.Ala999Ser
|
|
ENST00000456970.6:c.2820G>T
|
ENSP00000405002.2:n.2820G>T
|
|
ENST00000622290.4:c.*204G>T
|
ENSP00000483331.1:n.*204G>T
|
|
NM_001171.5:c.2995G>T
|
NP_001162.4:p.Ala999Ser
|
|
XM_011522479.1:c.2962G>T
|
XP_011520781.1:p.Ala988Ser
|
|
XM_011522480.1:c.2653G>T
|
XP_011520782.1:p.Ala885Ser
|
|
XM_011522481.1:c.2653G>T
|
XP_011520783.1:p.Ala885Ser
|
|
XR_932836.1:n.3230G>T
|
|
|
XR_932837.1:n.3231G>T
|
|
|
XR_932838.1:n.3231G>T
|
|
|
NM_001351800.1:c.2653G>T
|
NP_001338729.1:p.Ala885Ser
|
|
NR_147784.1:n.2857G>T
|
|
|
XM_011522479.2:c.2962G>T
|
XP_011520781.1:p.Ala988Ser
|
|
XM_011522481.3:c.2653G>T
|
XP_011520783.1:p.Ala885Ser
|
|
XM_017023212.1:c.2827G>T
|
XP_016878701.1:p.Ala943Ser
|
|
XM_017023214.1:c.2995G>T
|
XP_016878703.1:p.Ala999Ser
|
|
XM_024450261.1:c.3031G>T
|
XP_024306029.1:p.Ala1011Ser
|
|
XR_932836.2:n.3176G>T
|
|
|
XR_932837.3:n.3176G>T
|
|
|
XR_932838.3:n.3176G>T
|
|
|
NM_001171.6:c.2995G>T
MANE Select
|
NP_001162.5:p.Ala999Ser
|
|