ENST00000348931.9:c.471G>A
MANE Select
|
ENSP00000335384.5:p.Gly157=
|
|
ENST00000348931.8:c.471G>A
|
ENSP00000335384.5:p.Gly157=
|
|
ENST00000377940.3:c.405G>A
|
ENSP00000367174.3:p.Gly135=
|
|
ENST00000583811.5:c.117G>A
|
ENSP00000462463.1:p.Gly39=
|
|
ENST00000584588.5:c.407-710G>A
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ENSP00000462067.1:n.407-710G>A
|
|
NM_198844.2:c.405G>A
|
NP_942141.2:p.Gly135=
|
|
NM_199321.2:c.471G>A
|
NP_955353.1:p.Gly157=
|
|
XM_011524298.1:c.471G>A
|
XP_011522600.1:p.Gly157=
|
|
XR_002957959.1:n.662G>A
|
|
|
NM_198844.3:c.405G>A
|
NP_942141.2:p.Gly135=
|
|
NM_199321.3:c.471G>A
MANE Select
|
NP_955353.1:p.Gly157=
|
|