ENST00000334554.12:c.345G>C
MANE Select
|
ENSP00000334490.7:p.Pro115=
|
|
ENST00000320602.11:c.345G>C
|
ENSP00000317804.7:p.Pro115=
|
|
ENST00000334554.11:c.345G>C
|
ENSP00000334490.7:p.Pro115=
|
|
ENST00000405930.3:c.345G>C
|
ENSP00000384716.3:p.Pro115=
|
|
ENST00000436518.5:c.312G>C
|
ENSP00000412807.1:p.Pro104=
|
|
ENST00000468112.5:n.58-1021G>C
|
|
|
NM_001185024.1:c.345G>C
|
NP_001171953.1:p.Pro115=
|
|
NM_013373.3:c.345G>C
|
NP_037505.1:p.Pro115=
|
|
XM_006724239.2:c.345G>C
|
XP_006724302.1:p.Pro115=
|
|
NM_001185024.2:c.345G>C
|
NP_001171953.1:p.Pro115=
|
|
NM_013373.4:c.345G>C
MANE Select
|
NP_037505.1:p.Pro115=
|
|