ENST00000622290.5:c.3708G>T
|
ENSP00000483331.2:p.Met1236Ile
|
|
ENST00000205557.12:c.3708G>T
MANE Select
|
ENSP00000205557.7:p.Met1236Ile
|
|
ENST00000640696.1:c.522G>T
|
ENSP00000492197.1:p.Met174Ile
|
|
ENST00000205557.11:c.3708G>T
|
ENSP00000205557.7:p.Met1236Ile
|
|
ENST00000456970.6:c.3333G>T
|
ENSP00000405002.2:n.3333G>T
|
|
ENST00000622290.4:c.*917G>T
|
ENSP00000483331.1:n.*917G>T
|
|
NM_001171.5:c.3708G>T
|
NP_001162.4:p.Met1236Ile
|
|
XM_011522479.1:c.3675G>T
|
XP_011520781.1:p.Met1225Ile
|
|
XM_011522480.1:c.3366G>T
|
XP_011520782.1:p.Met1122Ile
|
|
XM_011522481.1:c.3366G>T
|
XP_011520783.1:p.Met1122Ile
|
|
XR_932836.1:n.3943G>T
|
|
|
XR_932837.1:n.3744G>T
|
|
|
XR_932838.1:n.3744G>T
|
|
|
XR_933134.1:n.539-272C>A
|
|
|
NM_001351800.1:c.3366G>T
|
NP_001338729.1:p.Met1122Ile
|
|
NR_147784.1:n.3370G>T
|
|
|
XM_011522479.2:c.3675G>T
|
XP_011520781.1:p.Met1225Ile
|
|
XM_011522481.3:c.3366G>T
|
XP_011520783.1:p.Met1122Ile
|
|
XM_017023212.1:c.3540G>T
|
XP_016878701.1:p.Met1180Ile
|
|
XM_024450261.1:c.3744G>T
|
XP_024306029.1:p.Met1248Ile
|
|
XR_932836.2:n.3889G>T
|
|
|
XR_932837.3:n.3689G>T
|
|
|
XR_932838.3:n.3689G>T
|
|
|
NM_001171.6:c.3708G>T
MANE Select
|
NP_001162.5:p.Met1236Ile
|
|