ENST00000265081.7:c.77G>A
(MSH3)
MANE Select
|
ENSP00000265081.6:p.Arg26Gln
|
|
ENST00000439211.7:c.-315C>T
(DHFR)
MANE Select
|
ENSP00000396308.2:n.-315C>T
|
|
ENST00000667069.1:c.77G>A
(MSH3)
|
ENSP00000499502.1:p.Arg26Gln
|
|
ENST00000670357.1:c.77G>A
(MSH3)
|
ENSP00000499791.1:p.Arg26Gln
|
|
ENST00000265081.6:c.77G>A
(MSH3)
|
ENSP00000265081.6:p.Arg26Gln
|
|
ENST00000439211.6:c.-315C>T
(DHFR)
|
ENSP00000396308.2:n.-315C>T
|
|
NM_000791.3:c.-315C>T
(DHFR)
|
NP_000782.1:n.-315C>T
|
|
NM_001290354.1:c.-421C>T
(DHFR)
|
NP_001277283.1:n.-421C>T
|
|
NM_001290357.1:c.-315C>T
(DHFR)
|
NP_001277286.1:n.-315C>T
|
|
NM_002439.4:c.77G>A
(MSH3)
|
NP_002430.3:p.Arg26Gln
|
|
NR_110936.1:n.178C>T
(DHFR)
|
|
|
NM_000791.4:c.-315C>T
(DHFR)
MANE Select
|
NP_000782.1:n.-315C>T
|
|
NM_002439.5:c.77G>A
(MSH3)
MANE Select
|
NP_002430.3:p.Arg26Gln
|
|
NM_001290354.2:c.-421C>T
(DHFR)
|
NP_001277283.1:n.-421C>T
|
|
NM_001290357.2:c.-315C>T
(DHFR)
|
NP_001277286.1:n.-315C>T
|
|
NR_110936.2:n.180C>T
(DHFR)
|
|
|