ENST00000622290.5:c.2950G>T
|
ENSP00000483331.2:p.Ala984Ser
|
|
ENST00000205557.12:c.2950G>T
MANE Select
|
ENSP00000205557.7:p.Ala984Ser
|
|
ENST00000205557.11:c.2950G>T
|
ENSP00000205557.7:p.Ala984Ser
|
|
ENST00000456970.6:c.2775G>T
|
ENSP00000405002.2:n.2775G>T
|
|
ENST00000622290.4:c.*159G>T
|
ENSP00000483331.1:n.*159G>T
|
|
NM_001171.5:c.2950G>T
|
NP_001162.4:p.Ala984Ser
|
|
XM_011522479.1:c.2917G>T
|
XP_011520781.1:p.Ala973Ser
|
|
XM_011522480.1:c.2608G>T
|
XP_011520782.1:p.Ala870Ser
|
|
XM_011522481.1:c.2608G>T
|
XP_011520783.1:p.Ala870Ser
|
|
XR_932836.1:n.3185G>T
|
|
|
XR_932837.1:n.3186G>T
|
|
|
XR_932838.1:n.3186G>T
|
|
|
NM_001351800.1:c.2608G>T
|
NP_001338729.1:p.Ala870Ser
|
|
NR_147784.1:n.2812G>T
|
|
|
XM_011522479.2:c.2917G>T
|
XP_011520781.1:p.Ala973Ser
|
|
XM_011522481.3:c.2608G>T
|
XP_011520783.1:p.Ala870Ser
|
|
XM_017023212.1:c.2782G>T
|
XP_016878701.1:p.Ala928Ser
|
|
XM_017023214.1:c.2950G>T
|
XP_016878703.1:p.Ala984Ser
|
|
XM_024450261.1:c.2986G>T
|
XP_024306029.1:p.Ala996Ser
|
|
XR_932836.2:n.3131G>T
|
|
|
XR_932837.3:n.3131G>T
|
|
|
XR_932838.3:n.3131G>T
|
|
|
NM_001171.6:c.2950G>T
MANE Select
|
NP_001162.5:p.Ala984Ser
|
|