ENST00000396373.9:c.1235G>T
MANE Select
|
ENSP00000379658.3:p.Gly412Val
|
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ENST00000266427.3:c.72G>T
|
|
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ENST00000396373.8:c.1235G>T
|
ENSP00000379658.3:p.Gly412Val
|
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NM_001987.4:c.1235G>T , LRG_609t1:c.1235G>T
|
NP_001978.1:p.Gly412Val
|
|
XM_011520607.1:c.1232G>T
|
XP_011518909.1:p.Gly411Val
|
|
XM_011520608.1:c.1208G>T
|
XP_011518910.1:p.Gly403Val
|
|
XM_011520609.1:c.971G>T
|
XP_011518911.1:p.Gly324Val
|
|
XM_011520610.1:c.971G>T
|
XP_011518912.1:p.Gly324Val
|
|
XM_011520611.1:c.971G>T
|
XP_011518913.1:p.Gly324Val
|
|
XM_011520612.1:c.614G>T
|
XP_011518914.1:p.Gly205Val
|
|
XM_011520607.2:c.1232G>T
|
XP_011518909.1:p.Gly411Val
|
|
XM_011520608.2:c.1208G>T
|
XP_011518910.1:p.Gly403Val
|
|
XM_011520609.2:c.971G>T
|
XP_011518911.1:p.Gly324Val
|
|
XM_011520611.2:c.971G>T
|
XP_011518913.1:p.Gly324Val
|
|
XM_011520612.2:c.614G>T
|
XP_011518914.1:p.Gly205Val
|
|
XM_017018990.1:c.1100G>T
|
XP_016874479.1:p.Gly367Val
|
|
XM_017018991.1:c.971G>T
|
XP_016874480.1:p.Gly324Val
|
|
NM_001987.5:c.1235G>T
MANE Select
|
NP_001978.1:p.Gly412Val
|
|