ENST00000586186.3:c.345+258G>C
|
ENSP00000468273.3:n.345+258G>C
|
|
ENST00000587405.6:c.3G>C
|
ENSP00000466478.2:p.Met1Ile
|
|
ENST00000590016.6:c.420G>C
|
ENSP00000466399.1:p.Met140Ile
|
|
ENST00000590631.2:n.437-627G>C
|
|
|
ENST00000592577.6:c.3G>C
|
ENSP00000466839.2:p.Met1Ile
|
|
ENST00000345365.11:c.360G>C
MANE Select
|
ENSP00000338790.6:p.Met120Ile
|
|
ENST00000335858.11:c.145-627G>C
|
ENSP00000338408.6:n.145-627G>C
|
|
ENST00000345365.10:c.360G>C
|
ENSP00000338790.6:p.Met120Ile
|
|
ENST00000394589.8:c.360G>C
|
ENSP00000378090.4:p.Met120Ile
|
|
ENST00000415064.6:n.510G>C
|
|
|
ENST00000460118.6:c.-125-47G>C
|
ENSP00000464356.2:n.-125-47G>C
|
|
ENST00000585343.5:c.442G>C
|
|
|
ENST00000585947.5:n.256G>C
|
|
|
ENST00000585982.5:n.500+258G>C
|
|
|
ENST00000586044.5:c.*91G>C
|
ENSP00000465584.1:n.*91G>C
|
|
ENST00000586186.2:c.248+258G>C
|
|
|
ENST00000586210.5:c.278G>C
|
ENSP00000465612.1:p.Trp93Ser
|
|
ENST00000587405.5:c.3G>C
|
ENSP00000466478.1:p.Met1Ile
|
|
ENST00000587977.5:c.*100G>C
|
ENSP00000466587.1:n.*100G>C
|
|
ENST00000587982.5:n.273+258G>C
|
|
|
ENST00000588372.5:c.3G>C
|
ENSP00000468764.1:p.Met1Ile
|
|
ENST00000588594.5:c.*76+258G>C
|
ENSP00000465366.1:n.*76+258G>C
|
|
ENST00000590016.5:c.420G>C
|
ENSP00000466399.1:p.Met140Ile
|
|
ENST00000590631.1:c.-51-627G>C
|
ENSP00000465033.1:n.-51-627G>C
|
|
ENST00000591723.5:c.-52+258G>C
|
ENSP00000467986.1:n.-52+258G>C
|
|
ENST00000592181.1:c.3G>C
|
ENSP00000464799.1:p.Met1Ile
|
|
ENST00000592430.5:n.329G>C
|
|
|
ENST00000592577.5:c.366G>C
|
ENSP00000466839.1:p.Met122Ile
|
|
ENST00000592850.5:c.346-627G>C
|
|
|
ENST00000592928.2:n.167-627G>C
|
|
|
ENST00000593039.5:c.4-627G>C
|
ENSP00000466834.1:n.4-627G>C
|
|
NM_001142571.1:c.420G>C
|
NP_001136043.1:p.Met140Ile
|
|
NM_002878.3:c.360G>C , LRG_516t1:c.360G>C
|
NP_002869.3:p.Met120Ile
|
|
NM_133629.2:c.145-627G>C
|
NP_598332.1:n.145-627G>C
|
|
NR_037711.1:n.497G>C
|
|
|
NR_037712.1:n.482+258G>C
|
|
|
NR_037714.1:n.233-627G>C
|
|
|
NM_001142571.2:c.420G>C
|
NP_001136043.1:p.Met140Ile
|
|
NM_133629.3:c.145-627G>C
|
NP_598332.1:n.145-627G>C
|
|
NR_037711.2:n.386G>C
|
|
|
NR_037712.2:n.371+258G>C
|
|
|
NM_002878.4:c.360G>C
MANE Select
|
NP_002869.3:p.Met120Ile
|
|